Good Laboratory Practices for Waived Testing Sites
Survey Findings from Testing Sites Holding a Certificate of Waiver Under
the Clinical Laboratory Improvement Amendments of 1988
and Recommendations for Promoting Quality Testing
Devery Howerton, PhD, Nancy Anderson, MMSc, Diane Bosse, MS, Sharon Granade, Glennis Westbrook
Division of Public Health Partnerships, National Center for Health Marketing, Coordinating Center for Health Information and Service
The material in this report originated in the Coordinating Center for Health Information and Service, Steven L. Solomon, MD, Director;
National Center for Health Marketing, Jay M. Bernhardt, PhD, Director; and the Division of Public Health Partnerships, Robert Martin, DrPH, Director.
Corresponding author: Devery Howerton, PhD, National Center for Health Marketing,
Coordinating Center for Health Information and Service;
4770 Buford Hwy NE, MS G-23, Atlanta, GA, 30341. Telephone:
770-488-8126; Fax: 770-488-8275; Email: email@example.com.
Under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), simple, low-risk tests can be waived
and performed with no routine regulatory oversight in physicians' offices and various other locations. Since CLIA was
implemented, waived testing has steadily increased in the United States. Surveys conducted during 1999--2004 by the Centers for
Medicare & Medicaid Services and studies funded by CDC during 1999--2003 evaluated testing practices in sites holding a
CLIA Certificate of Waiver (CW). Although study findings indicate CW sites generally take measures to perform testing
correctly, they raise quality concerns about practices that could lead to errors in testing and poor patient outcomes. These issues
are probably caused, in part, by high personnel turnover rates, lack of understanding about good laboratory practices,
and inadequate training. This report summarizes study findings and provides recommendations developed by the
Clinical Laboratory Improvement Advisory Committee for conducting quality waived testing. These recommendations
include considerations before introducing waived testing, such as management responsibility for testing, regulatory requirements,
safety, physical and environmental requirements, benefits and costs, staffing, and documentation. They also cover good
practices for the three phases of testing: 1) before testing (test ordering and specimen collection), 2) during testing
(control testing, test performance, and result interpretation and recording), and 3) after testing (result reporting,
documentation, confirmatory testing, and biohazard waste disposal). They are intended to be used by those who would benefit from
improving their knowledge of good laboratory practices. Continued monitoring of waived testing, with a focus on personnel education
and training, is needed to improve practices and enhance patient safety as waived testing continues to increase.
Laboratory testing plays a critical role in health assessment, health care, and ultimately, the public's health. Test
results contribute to diagnosis and prognosis of disease, monitoring of treatment and health status, and population screening
for disease. Laboratory testing affects persons in every life stage, and almost everyone will experience having one or
more laboratory tests conducted during their lifetime. An estimated
7--10 billion laboratory tests are performed each year in
the United States (1,2), and laboratory test results influence approximately 70% of medical decisions
(2--4). Increasingly, these decisions are based on simple tests performed at the point-of-care using devices that are waived from most federal
oversight requirements (and are thus designated as waived tests), including
requirements for personnel qualifications and
training, quality control (QC) (unless specified as required in the test system instructions), proficiency testing (PT), and routine
Advances in technology have made tests simpler, contributing to this shift in testing. In the past, tests such as
prothrombin time, cholesterol, and glucose either used complex manual methodologies or were performed using sizable
instrumentation suitable for use by highly trained personnel in traditional clinical laboratory settings. Many tests can now be performed
using compact or hand held devices by personnel with limited experience and training. These advances have enabled more testing
be performed in emergency departments, hospital rooms, and physicians' offices and in nontraditional testing sites such
as community counseling centers, pharmacies, nursing homes, ambulances, and health fairs. Since the 1992
inception of the program implementing the Clinical Laboratory Improvement Amendments of 1988 (CLIA), the numbers of waived tests
and the sites that perform them have increased dramatically. This trend is expected to continue as laboratory testing
technology continues to evolve.
The purpose of this report is to highlight quality issues identified in waived testing sites on the basis of surveys
conducted on-site by the Centers for Medicare & Medicaid Services (CMS) during 1999--2004 and studies of waived testing
practices funded through CDC during 1999--2003. In addition, this report presents recommendations developed by the
Clinical Laboratory Improvement Advisory Committee (CLIAC) for improving the quality of waived testing. By following
these recommendations, errors that could potentially lead to
patient harm and the associated morbidity and mortality can
CLIA Requirements for Waived Testing
All facilities in the United States that perform laboratory testing on human specimens for health assessment or the
diagnosis, prevention, or treatment of disease are regulated under CLIA
(5). The CLIA program is administered by CMS and
is implemented through three federal agencies---CDC, CMS, and the Food and Drug Administration (FDA). When CLIA
was implemented in 1992, CLIAC was chartered to provide scientific and technical advice and guidance to the U.S.
Department of Health and Human Services (HHS) about laboratory standards and their impact on medical and laboratory practice.
The committee consists of 20 members selected by the HHS secretary from authorities knowledgeable in the fields of
laboratory medicine, pathology, public health, and clinical practice and includes consumer representatives and an industry
liaison. CLIAC also includes three ex officio members from CDC, CMS, and FDA.
By law, CLIA regulations are based on a complexity model, with more complicated testing subject to more
stringent requirements (6). The three categories of testing for CLIA purposes are waived, moderate complexity (including the
provider-performed microscopy procedures [PPMP] subcategory), and high complexity. Facilities performing only waived tests have
no routine oversight and no personnel requirements and are only required to obtain a Certificate of Waiver (CW), pay
biennial certificate fees, and follow manufacturers' test instructions.
Tests can be waived under CLIA if they are determined to be "simple tests with an insignificant risk of an erroneous
result" (5). Eight tests were included in the 1992 CLIA regulations (a ninth test was subsequently added) as meeting these criteria
and later, the FDA Modernization Act of 1997 clarified that tests cleared by FDA for home use are automatically waived.
An additional route to waiver exists through a process in which FDA evaluates studies and other information submitted
by manufacturers to demonstrate that a test meets the waiver criteria of being simple and having a low risk for
error. Approximately 1,600 test systems representing at least 76 analytes are waived under CLIA
Scope of Waived Testing
Sites performing only waived tests comprise 58% (105,138) of the approximately 180,000 laboratory testing sites in
the United States (Table 1, Figure 1). Waived testing performed in these sites is often wellness testing, screening tests, or
other critical testing that introduces a large population of persons into the health-care setting. Although the testing performed
in CW sites accounts for <10% of the total U.S. testing volume, this percentage has been increasing each year since the
CLIA program began (Table 1). Most testing is not waived and is typically performed in hospital or reference
laboratories (Certificate of Compliance and Certificate of Accreditation), which comprise 20% of the total number of testing sites
(Figure 1). The remaining testing sites (22%) have PPMP certificates, meaning that in addition to waived tests, direct
microscopic examinations of certain specimens can be performed as part of the patient's examination by that patient's physician or
midlevel health-care practitioner. An increasing shift toward waived testing has resulted in a corresponding increase in
health-care expenditures for this testing. Medicare Part B, the federal medical insurance program for persons aged
>65 years and certain disabled persons, covers diagnostic laboratory testing. Payment data for 2004, provided by CMS, indicated that of
the $3,494,840,086 spent on reimbursed laboratory testing for that year, $128,169,398 (3.7%) was for waived tests. The
of Medicare Part B reimbursed waived laboratory testing in 2004 represented 8% of the total reimbursed testing volume
for that year, a 57% increase over the volume in 2000 (Table 1).
Patient Safety Concerns Related to Waived Testing
Efforts to reduce medical errors, improve health-care quality, and increase patient safety have been gaining
national attention. A report issued in 1999 by the Institute of Medicine (IOM) presented a national agenda to address these
issues and recommended strategies for change that included the implementation of safe practices at the health-care delivery level
(7). As described in the IOM report, errors most often occur when multiple contributing factors converge, and preventing errors
and improving patient safety require a systems approach. Five years after this seminal report, small but consequential changes
have occurred that have shifted the focus to improving systems, engaging stakeholders, and motivating health-care providers
to adopt new safe practices (8).
Although by law waived tests should have insignificant risk for erroneous results, these tests are not completely
error-proof and are not always used in settings that employ a systems
approach to quality and patient safety. Errors can occur anywhere
in the testing process, particularly when the manufacturer's instructions are not followed and when testing personnel are
not familiar with all aspects of the test system and how testing is integrated into the facility's workflow. Although data have
not been systematically collected on patient outcomes with waived testing, adverse events can
occur (9). Some waived tests have potential for serious health impacts if performed incorrectly. For example, results from waived tests can be used to
adjust medication dosages, such as prothrombin time testing in
patients undergoing anticoagulant therapy and glucose monitoring
in diabetics. In addition, erroneous results from diagnostic tests, such as those for
human immunodeficiency virus (HIV) antibody, can have
The lack of oversight and requirements for personnel qualifications and training for an increasingly large number of
CW sites is a concern and could contribute to errors and patient harm. During 1999--2001, CMS conducted on-site surveys of
a representative sample of CW sites in 10 states to assess the quality of testing in these sites. These pilot surveys
identified quality issues that could result in medical errors
(10). Contributing factors included inadequate training in good
laboratory practices and high turnover rates of testing personnel. As a result, during 2002--2004, CMS conducted nationwide
on-site surveys of CW facilities to collect additional data that would provide an assessment of testing, promote good
laboratory practices and encourage improvement through educational outreach, and make recommendations on the basis of
cumulative survey findings. The data collected from these surveys, along with data on waived testing practices gathered through
CDC-funded studies conducted during 1999--2003 by the state health departments of Arkansas, New York, and
Washington (collectively referred to as the Laboratory Medicine Sentinel Monitoring Network [LMSMN]), support the initial
CMS findings of gaps in good laboratory practices in these sites
(11--16). In addition, a 2001 report issued by the HHS Office
of Inspector General (OIG), following their investigation of CLIA certification and enrollment processes, identified the lack
of routine on-site visits to CW sites by surveyors representing state agencies and private sector accreditation organizations
as presenting vulnerabilities in these sites. The OIG report indicated that approximately half of the state respondents
reported problems related to quality issues with the waived laboratories in their states (e.g., failure to follow manufacturers'
instructions or failure to identify incorrect results
and performing unauthorized testing) (17). The concerns noted by states were similar
to those identified in the CMS pilot studies.
An initial CMS report of its 2002--2003 survey findings, presented to CLIAC in 2004, supported earlier concerns about
the quality of testing practices and the need for education and training of testing personnel in CW sites. In response,
the committee recommended publication of the 2002--2004 CMS data in conjunction with other data pertinent to waived
testing performance along with recommendations for good laboratory practices for waived testing sites. This information would
then be available to provide guidance to physicians, nurses, and other health-care providers in CW facilities. As a result,
a workgroup was appointed to consider practices associated with the waived testing process and their impact on the quality
of waived testing. This workgroup was comprised of key stakeholders in waived testing (i.e., CLIAC members; physicians;
nurses; laboratorians; manufacturers; distributors; and representatives from CDC, CMS, and FDA). In its evaluations, the
workgroup considered existing practice guidelines from professional organizations, waived testing recommendations from CMS,
and professional experience, and publications related to waived testing. The workgroup's findings were presented to
CLIAC for its deliberations at the February 2005 meeting, at which time CLIAC provided recommendations to HHS
concerning good laboratory practices for waived testing sites. CLIAC supported publication of the recommendations, along with the
data from the studies of CW sites, and suggested the publication could serve as a comprehensive source document that could
be used to develop additional educational tools appropriate for specific target audiences.
Surveys of Waived Testing Sites
During 2002--2004, approximately 150 CMS and state agency surveyors conducted on-site surveys nationwide using
a questionnaire at 4,214 sites performing testing under a CLIA CW. Surveyors self-selected CW sites on the basis of
test volume, location, and facility types. Different facilities were surveyed each year so that no repetition exists among CW
sites represented in the CMS data in this report. LMSMN obtained additional waived testing data from 1999--2003.
Within LMSMN, the Washington State Department of Health
established the Pacific Northwest Sentinel Network (PNWSN),
which included approximately 650 waived and nonwaived laboratories in Alaska, Idaho, Oregon, and Washington. The
Arkansas Sentinel Network (ASN) consisted of 94 local health units integrated into the state health agency (mostly waived testing
sites) and approximately 600 waived and nonwaived laboratories in Arkansas and surrounding states. PNWSN and ASN
gathered data about waived testing practices through questionnaires mailed to network members
(11). The New York Sentinel Network (NYSN) consisted of approximately 600 limited service laboratories (facilities other than physician office laboratories
[POLs] that perform only waived tests and PPMP). NYSN collected its data through on-site surveys during which waived
testing practices were assessed by surveyor observation and record reviews
CMS surveyed 4,214 CW sites during April 15, 2002--November 12, 2004. This included 897 sites in 2002, 1,575 sites
in 2003, and 1,742 sites in 2004. Of the CW facility types surveyed, POLs compose the largest percentage (47%), followed
by skilled nursing facilities (14%) (Table 2). The CW sites surveyed estimated performing a broad range of annual test
volumes (Figure 2). Of the facilities surveyed by CMS during 2003--2004 (2002 data not available), 90%
reported that they performed no more than five different waived tests, and 99% performed no more than 10 different waived tests. Although
the exact volume of each test performed per site is not known, on the basis of the number of sites testing for each analyte, the
five most commonly performed waived tests were identified as glucose, dipstick urinalysis,
fecal occult blood, urine human chorionic gonadotropin (hCG) (visual color comparison), and group A streptococcal antigen (direct test from throat
swabs) (Figure 3). This correlates with data for the top five waived tests identified through the LMSMN, especially for POLs
(11). Although not among the most commonly performed, waived tests are available for certain infectious diseases of public
health significance and were reportedly performed by CW sites in the CMS surveys (influenza, 46 sites; HIV, four; and Lyme
Personnel and Training
Under CLIA, no education or training is required for the director or testing personnel in CW sites. The
educational background and qualifications for directors and testing personnel at CW sites were collected as part of the CMS surveys
and by LMSMN (PNWSN and NYSN). The CMS surveys indicated that in 69% of CW sites, physicians served as
directors, followed by nurses (17%) (Table 3). Similarly, 59% of the PNWSN CW site directors were physicians, with
the remaining 41% having other backgrounds or degrees
(12). For CW testing personnel, according to the CMS data, the
top four categories were nurses (46%), medical assistants (25%), physicians (9%), and high school graduates (7%) (Table 3). NYSN reported that registered nurses (RNs) and licensed practical nurses (LPNs) served as testing personnel in 84% of
the limited service laboratories they surveyed
(13). Trained laboratorians (i.e., medical technologists and medical
laboratory technicians) accounted for 2% of laboratory directors and testing personnel in the CW sites surveyed by CMS and a
smaller percentage in the limited service laboratories surveyed by the NYSN
CMS surveys indicated that 43% of CW sites experienced a change in testing personnel during the preceding 12
months. Among the top categories of testing personnel in the PNWSN, turnover rates were highest for medical assistants (17%),
followed by LPNs (13%), RNs (9%), and physicians (2%)
(14). Although the majority of CW sites in the CMS surveys (90%)
reported that new personnel were trained, fewer sites (85%) evaluated staff to
ensure competency. Data identifying who provided
training were not submitted for all sites in the surveys. However, according to the CW sites that provided this information for
2003--2004 (Table 4), nurses most frequently provided waived test training (33%), followed by the manufacturer or sales
representatives (15%). Findings from a PNWSN study indicated that the highest percentage of personnel were initially trained by
another employee (25%) or trained themselves by using instructions provided with the waived test system (17%)
(15). Another PNWSN study indicated that most training (77%) took place in a day or less
(14). Comments from this study reflected the thinking
that training is not always necessary or that minimal time should be spent on training because persons have been trained in school
or on other jobs. The time spent on training was not captured as part of the CMS surveys.
The CMS surveys indicated that the majority of the CW sites were aware of and followed some practices for ensuring
the accuracy and reliability of their testing. However, lapses in quality were identified at certain sites, some of which could
result in patient harm. In some instances, CW sites were determined to be performing testing that was an imminent and
serious threat to the public's health because they were performing nonwaived testing in the
absence of CLIA-required quality measures. The CMS surveys indicated that 5% of CW sites were conducting tests that were not waived, the most
frequently performed nonwaived procedures (72%) being direct microscopic examinations (e.g., potassium hydroxide preparations,
wet mounts, or urine sediment examinations). Surveyed CW testing sites also reported performing various other nonwaived
tests (e.g., urine and throat cultures, Rh antigen testing, and the use of glucometers to perform diagnostic glucose tolerance
testing [an intended use not specified in manufacturers' instructions]). When performing nonwaived tests, surveyors noted that,
in some instances, the sites were not meeting CLIA requirements for qualified personnel, QC, PT, or test system maintenance.
In addition, these sites did not have adequate records of their testing activities, including test system procedures, training
records, or other documentation.
Of the CW facilities CMS surveyed, 12% did not have the most recent instructions for the waived test systems they
were using, and 21% of the sites reported they did not routinely check the product insert or instructions for changes to
the information (Table 5). On the basis of manufacturer's instructions, 21% of the CW sites did not perform QC testing
as specified, and 18% of the sites did not use correct terminology or units of measure when reporting results. Among
other quality deficiencies identified were failure to adhere to proper expiration dates for the test system, reagents, or
control materials (6%) and failure to adhere to the storage conditions as described in the product insert (3%). Six percent of CW
sites did not perform follow-up confirmatory tests as specified in the instructions for certain waived tests (e.g., group
A streptococcal antigen), and 5% did not perform function checks or calibration checks to ensure the test system was
operating correctly. Findings from the LMSMN studies were similar to the CMS findings for these quality deficiencies
Although not usually specified in the product insert (and therefore not a CLIA requirement), proper documentation
and recordkeeping of patient and testing information are also important elements of good laboratory practices. CMS
surveys indicated that 45% of CW sites did not document the name, lot number, and expiration dates for tests performed; 35%
did not maintain logs with records of their QC testing; 31% did not maintain a log or record of tests performed; and 9% did
not require a requisition or test orders documented in a patient chart before performing a test (Table 5). NYSN
observed similar findings but noted increased compliance with state requirements for documentation/recordkeeping when laboratories
had formal affiliations with New York State-licensed
The findings from the CMS surveys and LMSMN studies indicated that the majority of CW testing sites performed
testing correctly and provided reliable service. However, in CW sites, most directors and testing personnel did not have
formal laboratory training or testing experience, there was a high turnover of personnel, and lapses in following
manufacturers' instructions and instituting practices to ensure the quality of the testing were noted. The survey findings indicated that
485 (12%) of the 4,214 CW sites surveyed did not have the current manufacturers' instructions available, and 701 (21%) of
the 3,317 sites surveyed during 2003--2004 did not check to be sure there had been no changes to the instructions. Test
instructions can change over time and CW sites sometimes switch test systems that could have different instructions.
CMS survey results also indicated that, in varying proportions, when CW sites had the current instructions, they did not
follow critical steps in the testing process (e.g., performing QC testing, reporting results correctly, adhering to expiration dates
and appropriate storage requirements, and performing test system function checks or calibration checks). This is a concern
because the only CLIA requirement for performing waived testing is to follow the manufacturer's instructions. Neglecting to
follow instructions could cause inaccurate test results that could lead to incorrect diagnoses, inappropriate or unnecessary
medical treatment, and poor patient outcomes.
CMS surveys indicated that certain CW sites (5%) were performing testing more complex than waived testing without
taking required measures to ensure quality. In certain
CW sites, nonwaived microscopic examinations were being performed
by personnel who lacked the education and training needed to develop the interpretive and judgment skills necessary to
accurately perform these procedures. In addition, measures such as QC, PT, adequate documentation, and monitoring are required
to ensure the accuracy and reliability of nonwaived test results. Although direct microscopic examinations can be conducted by
a physician or midlevel health-care practitioner as part of a patient examination, testing must be conducted under a CLIA
The quality issues identified through these surveys might have been caused, in part, by high turnover rates of
testing personnel in CW sites, inadequate training with respect to waived testing, and lack of understanding of good
laboratory practices, including the importance of following all aspects of the manufacturers' instructions. Although the study
results indicated that most testing personnel were trained, they were often trained for minimum periods by persons who did not
have formal education or training in clinical laboratory testing and who might not have understood the importance of measures
to ensure quality testing. Certain testing personnel also were self-trained. In addition, when testing personnel were not
evaluated to determine their competency level following training or on an ongoing basis, no assessment was conducted to
determine whether the training was effective. The data demonstrate a need for educational information among CW site directors
and testing personnel about the importance of following manufacturers' instructions, adhering to expiration dates, performing
QC testing, and proper documentation and recordkeeping. One of the recommendations in the 2001 OIG report was that
CMS should provide educational outreach to directors of waived and PPMP laboratories about the CLIA requirements
The findings in the 2002--2004 CMS surveys are subject to at least three limitations, and caution should be used
in extrapolating the survey data to make generalizations about waived testing. First, the CMS surveys were not intended to be
a scientific study of a random sample of CW sites. Waived testing data were collected by CMS to provide an assessment
of testing practices, promote good laboratory practices, and encourage improvement through educational
outreach. Although surveyors attempted to include a wide variety of CW sites in the sample, the sites were self-selected by surveyors
and selection was based, to some degree, on convenience to the surveyors and willingness of the sites to participate in the
voluntary surveys. However, few sites refused to participate in the surveys. Overall, the sites represent a nationwide sample and
the distribution of CW facility types is similar to the distribution of CW facility types in the United States
(Table 2). In addition, the 2002--2004 CMS survey findings resulted in the same general conclusions as the earlier CMS pilot studies, which
were conducted on a random sample of laboratories
(10). Second, the CMS data were collected and entered into the database by
a large number of persons, introducing variability. Although training was provided before the surveys were conducted, the
intent of the survey questions was subject to individual interpretation. Because the phrasing of some questions differed slightly
from 2002 to 2003--2004, in certain cases, the meanings of the questions also changed. Finally, the CMS surveys did not assess
the frequency of erroneous test results in CW sites or whether lapses in following manufacturers' instructions directly affected
test results or patient outcomes. Similar limitations to these were identified in the LMSMN studies
The findings of the CMS and LMSMN studies are strikingly similar. Even though the majority of CW sites meet the
CLIA requirement to follow manufacturers' instructions for test performance, and many sites follow additional good
laboratory practices, over the years these studies have demonstrated that a persistent percentage of CW sites do not meet
minimal requirements and are not aware of recommended practices to help ensure quality testing. Because surveying all CW sites is
not feasible, the proposed actions to improve and promote quality testing in CW sites emphasize the importance of education
and training for CW site directors and testing personnel. To provide a guide that can be adapted for use, either in part or as
a whole, by persons or facilities considering the initiation of waived testing and personnel performing waived testing,
CLIAC provided recommendations for good laboratory practices. By implementing these recommendations, CW sites could
improve quality, reduce testing errors, and enhance patient safety.
Recommended Good Laboratory Practices
These recommendations are intended to promote the use of good laboratory practices by physicians, nurses, and
other providers of waived testing in a variety of CW sites. They were developed on the basis of recommendations and
other resources that provided additional information for promoting patient safety and the quality of CLIAC waived testing
in laboratories or nontraditional testing sites
(18--22). These recommendations address decisions that need to be made and
steps to be taken as a facility begins offering waived testing or adds a new waived test. They also address developing procedures
and training CW personnel and describe recommended practices for each phase of the total testing process, or path of
workflow, including the important steps or activities before, during, and after testing. The activities that occur in each of these phases
are critical to providing quality testing (Table 6).
Considerations Before Introducing Waived Testing or Offering a New Waived Test
Forethought, planning, and preparation are critical to initiating high-quality waived testing in any type of setting.
This section describes factors to consider before opening a waived testing site or offering an additional waived test. Questions
to address include the following:
- Management responsibility for testing. Who will be
responsible and accountable for testing oversight at the CW site,
and does this person have the appropriate training for making decisions on testing?
- Regulatory requirements. What federal, state, and local regulations apply to testing, and is the site adequately prepared
to comply with all regulations?
- Safety. What are the safety considerations for persons conducting testing and those being tested?
- Testing space and facilities. What are the physical and environmental requirements for testing?
- Benefits and costs. How will the care offered in the site benefit by introduction of testing or the addition of a new
test, and what will it cost?
- Staffing. How will introduction of testing affect the current work flow, are there sufficient personnel to conduct
testing, and how will they be trained and maintain testing competency?
- Documents and records. What written documentation will be needed, and how will test records be maintained?
Each testing site should identify at least one person responsible for testing oversight and decision-making, later referred to
as the CW site director. In POLs, this might be a physician or someone in a senior management position who has
the appropriate background and knowledge to make decisions about laboratory testing. Ideally, the person signing the
CW application (CMS Form 116) is responsible for management of the testing operations. The management staff
should demonstrate a commitment to the quality of testing service by complying with applicable regulatory requirements
and promoting good laboratory practices.
CLIA certification. Each site offering only waived testing that is not included under any other type of CLIA
certificate must obtain a CLIA CW before testing patient specimens. Certain sites offering waived testing can be certified as part of
a larger health-care organization that holds a CLIA Certificate of Compliance or Certificate of Accreditation. In
addition, certain public health testing sites offering only waived testing can be included under a limited public health or
mobile testing exception. A valid CLIA certificate is required for Medicare reimbursement.
To apply for a CLIA certificate, CMS Form 116 (http://www.cms.hhs.gov/clia/cliaapp.asp) must be completed and sent
to the state agency for the state in which the testing site is located. This form asks for specific information, including the type
of testing site (laboratory type), hours of operation, estimated total annual volume of waived testing, and the total number
of persons involved in performing waived testing. The form must be signed by the facility owner or the facility director.
Specific state agencies and contacts are available at
http://www.cms.hhs.gov/clia/ssa-map.asp. The state agency will process
the application and send an invoice for the registration fee. If additional assistance is required, contact the
appropriate CMS regional office (http://www.cms.hhs.gov/clia/ro-map.asp).
CLIA requirements that apply to testing sites operating under a CW include the following:
- Renew the CW every 2 years.
- Perform only waived tests. Waived tests include test systems cleared by FDA for home use, and simple, low-risk
tests categorized as waived under CLIA. Sometimes a test that can be performed using different specimens or procedures
might be waived only for certain specimen types or procedures. Because the list of waived tests is constantly being revised as
new test systems are added, the most current information about waived tests and appropriate specimens is available at
- Follow the instructions in the most current manufacturer's product insert, without modification, when performing
the test. Changes to the timing of the test or physical alteration of the test components (e.g., cutting test cards or strips
to increase the number of specimens tested per kit) are examples of modifications. If modified, tests are no longer
waived tests and become subject to the more stringent CLIA requirements for nonwaived testing.
- Permit announced or unannounced on-site inspections by CMS representatives.
State and local regulations. States and local jurisdictions vary as to the extent to which they regulate laboratory
testing. Some states and localities have specific regulations for testing, some require licensure of personnel who perform testing,
and some have phlebotomy requirements. State and local jurisdictions often regulate biohazard safety, including handling
and disposal of medical waste. The person responsible for testing oversight should ensure that all state and local requirements
are met. These requirements might be more or less stringent than federal requirements. When state or local regulations
governing laboratory testing are more stringent than the federal CLIA requirements, they supersede what is required
Safety requirements. The Occupational Safety and Health Administration (OSHA) and individual state standards
require employers to provide a safe and healthy work environment for employees. Each CW site must comply with OSHA
standards pertinent to workplace hazards
(23). Regulatory requirements for all OSHA standards, including specific information
for medical and dental offices (24), are available at
http://www.osha.gov and by telephone, 800-321-6742.
The OSHA Bloodborne Pathogens Standard applies to sites where workers have potential occupational exposure to
blood and infectious materials (25). The requirements for compliance with this standard include, but are not limited to:
Additional safety practices for performing testing are:
- A written plan for exposure control, including postexposure evaluation and follow-up for the employee in the event of
an "exposure incident;"
- Use of Universal Precautions, an approach to infection control in which all human blood and certain human body
fluids are treated as if known to be infectious for HIV, hepatitis B virus, hepatitis C virus, and other bloodborne
pathogens. Universal Precautions is one component of Standard Precautions, a broader approach designed to reduce the risk
for transmission of microorganisms from both recognized and unrecognized sources of infection in hospitals;
- Use of safer, engineered needles and sharps;
- Use of personal protective equipment (PPE) such as gloves and protective eyewear;
- Provision of hepatitis B vaccination at no cost for those with possible occupational exposure who want to be vaccinated;
- Safety training for handling blood, exposure to bloodborne pathogens, and other infectious materials; and
- Equipment for the safe handling and disposal of biohazardous waste (e.g., properly labeled or color-coded
sharps containers and biohazard trash bags and bins).
- Prohibit eating, drinking, or applying makeup in areas where specimens are collected and where testing is being
performed (i.e., where hand-to-mouth transmission of pathogens can occur);
- Prohibit storage of food in refrigerators where testing supplies or specimens are stored;
- Provide hand-washing facilities or antiseptic
hand-washing solutions; and
- Post safety information for employees and patients.
Specific information on the Bloodborne Pathogens Standard and needlestick prevention is available at
CDC and the Clinical and Laboratory Standards Institute (CLSI) (formerly NCCLS) have also published
information about biosafety and precautions for preventing transmission of bloodborne pathogens in the workplace
Privacy and confidentiality requirements. The Health
Insurance Portability and Accountability Act of 1996
(HIPAA) established federal privacy standards to protect patients' medical records and other health information provided to
health plans, doctors, hospitals, and other health-care providers. Under HIPAA, CW sites are required to establish policies
procedures to protect the confidentiality of health information about their patients, including patient identification,
test results, and all records of testing. These medical records and other individually identifiable health information must
be protected, whether on paper, in computers, or communicated orally. In addition, CW sites should be aware that
applicable state laws that provide more stringent privacy protections for patients supersede HIPAA. Additional information on HIPAA
is available at http://www.hhs.gov/ocr/hipaa.
Physical Requirements for Testing
Testing should be performed in a separate designated area where adequate space to safely conduct testing and
maintain patient privacy is available. In addition, some tests have specific environmental requirements described in the
manufacturer's product insert that need to be met to ensure reliable test results. Meeting these environmental conditions can be challenging
in nontraditional settings (e.g., health fairs) or community outreach venues (e.g., shopping malls, meeting rooms, parks,
parking lots, mobile vans, and buses). Factors to consider include:
- Humidity --- Unusually high, low, or extreme fluctuations in humidity can cause deterioration of reagents and
test components, affect the rate of chemical reactions and specimen interaction, or make test endpoints blurred and
difficult to read.
- Temperature --- Temperature ranges for storage of test components and controls and for test performance are defined
by the manufacturer to maintain test integrity. Extreme temperatures can degrade reagents and test components,
impact reaction times, cause premature expiration of test kits, and affect the test results.
- Lighting --- Inadequate lighting can negatively affect specimen collection, test performance, and interpretation of
- Work space --- Work surfaces should be stable and level and be able to be adequately disinfected; work space should
be adequate in size for patient confidentiality, ease of specimen collection, test performance, and storage of supplies
Benefit and Cost Considerations
Evaluating the benefits of a particular test. Evaluate the test system, its intended use, performance characteristics, and
the population to be tested when assessing whether to introduce waived testing or a new waived test. Information for
this evaluation can be obtained from the test manufacturer's product insert
(Table 7) or by speaking with the manufacturer's technical representatives. Specific considerations include:
- Intended use -- Be aware of the intended medical use for which FDA approved the test system as explained in the
product insert. This section describes what is being measured by the test, the type of specimen for which it is approved,
and whether it is a quantitative or qualitative measurement.
- Performance characteristics --- Assess the information on performance provided by the test manufacturer or
published data. Review data that includes the test's accuracy, precision, sensitivity, specificity, and interferences.
- Patient population --- Consider the population that will be tested before offering a test. Some tests have not
been evaluated for use in specific age groups (e.g., pediatric populations). The predictive value for certain types of test results
in a specific patient population depends on the test's sensitivity, specificity, and the prevalence of the condition in
the population. For example, when testing for a certain condition or disease in a low-prevalence population, the
predictive value of a positive result will be low compared with the predictive value of a negative result. Refer to the product insert
for limitations for use in particular patient populations.
- Need for supplemental testing or patient follow
up --- Some waived tests provide preliminary results as part of a
multitest series (e.g., rapid HIV testing) or results that must be considered in conjunction with other medical information.
These test results might require additional testing before a definitive test result is obtained, and
patients might need posttest counseling about the meaning of the test result. Assess the potential need for additional time, documentation, and
staffing and a mechanism to refer additional testing to another laboratory when
offering such tests.
- Test system considerations ---
Consider the simplicity of operating the test system, length of time to obtain a
result, and the level of technical support provided by the manufacturer or distributor. Sales restrictions, such as special
training requirements, development of a quality assurance program, or provision of information to patients, might apply to
some waived tests and require additional planning and resources.
Cost considerations. A fiscal assessment of testing is part of a good management program. Before offering a new
test, consider the level of reimbursement and factors that contribute to total test cost. These factors include:
- Test kits or instruments, supplies not provided with the test, control and calibration materials, inventory requirements
for anticipated test volume (including seasonal testing), and the shelf life of test components and supplies.
- Equipment maintenance, such as repairs or preventive maintenance contracts.
- Additional safety and biohazard equipment.
- Personnel training, competency assessment, and the
potential need for additional personnel.
- Recordkeeping and information systems.
- Required supplemental/confirmatory testing.
- Regulatory compliance.
- Resource needs to manage public health reporting, if
required nationally or by the state.
Personnel competency and turnover are important factors affecting the quality and reliability of waived testing results.
No CLIA requirements exist for waived testing personnel qualifications; however, applicable state or local personnel
regulations must be met. Personnel issues to consider include:
Developing Procedures and Training Personnel
- Is staffing adequate?
--- Determine whether employees have sufficient time and skills to reliably perform all activities needed for testing
in addition to their other duties.
--- Be aware that temporary or parttime personnel might be less proficient in performing testing.
--- Evaluate staff for color-blindness because this can limit their ability to interpret test results based on color endpoints.
- How much training will be needed?
--- Take into account the staff turnover rate and the
ongoing need to provide training for new personnel.
--- Factor in the time and resources for adequate training and competency evaluation of staff before they perform testing.
--- Consider how testing personnel will maintain competency, especially when testing volume is low.
After the decision is made to offer waived testing, it is good practice to develop written policies and procedures so
that responsibilities and testing instructions are clearly described for the testing personnel and facility director. The
testing procedures form the basis of training for testing personnel. These procedures should be derived from the
manufacturer's instructions and should be in a language understandable to testing personnel.
Written Test Procedures
To comply with CLIA requirements and provide accurate testing, CW sites must adhere to the manufacturer's
current testing instructions. These instructions, as outlined in the product insert, include directions for specimen collection
and handling, control procedures, test and reagent preparation, and instructions for test performance, interpretation, and
reporting (Table 7). In addition, certain manufacturers provide quick reference instructions formatted as cards or small signs
containing essential steps in conducting a test. Quick reference instructions should be clearly posted where testing is performed.
The specific test system name should be on the quick reference instructions to avoid confusion.
A comprehensive procedure manual is a valuable resource for CW sites. Although product inserts can be used as
test procedures, these instructions will typically need to be supplemented with testing information that is unique to the CW
site's operations and workflow (31). A procedure manual can also include examples of forms used (e.g., charts to record daily
test kit storage temperatures, infectious disease reporting forms, or logs for recording control testing and test
results) and check lists for personnel training. New testing procedures should be reviewed and signed by the CW site director
before incorporating them into the procedure manual. The manual should be updated as tests or other aspects of the testing
service change and should be reviewed by the director whenever changes are made. When procedures are no longer used, they
should be removed from the manual and retained with a
notation of the dates during which they were in service.
When writing procedures for each CW site, it might be helpful to:
- Use a template with standard component headings to
facilitate writing a new procedure and promote ease of use
when performing testing;
- List all materials needed and how to prepare them before testing;
- Include instructions for patient preparation and specimen collection;
- Highlight key steps in the procedure (e.g., test incubation time);
- List test limitations;
- Describe actions to take when the test does not perform as expected;
- Integrate control procedures with the steps for performing patient testing to assure control testing is performed;
- Include established reference intervals and critical values for the test; and
- Describe how to record and report results and how to handle critical values.
Trained and competent testing personnel are essential to good quality testing and patient care. Data from CDC and
CMS surveys demonstrate that waived testing sites are subject to a high rate of personnel turnover. Personnel should be trained
and competent in each test they will perform before reporting patient results
(32,33). In addition, training should include
aspects of safety (including Universal Precautions) and
QC. The CW site director or other person responsible for overseeing
testing should ensure that testing personnel receive adequate training and are competent to perform the procedures for which they
are responsible. Training checklists are helpful to ensure the training process is comprehensive and documented.
The training process. Training should be provided by a qualified person (e.g., experienced co-worker, facility expert,
or outside consultant) with knowledge of the test performance, good laboratory practices, and the ability to evaluate the
efficacy of the training. On-the-job training should include the following steps:
- The trainee reads the testing instructions.
- The trainer demonstrates the steps for performing the test.
- The trainee performs the test while the trainer observes.
- The trainer evaluates test performance, provides feedback and additional instruction, and follow-up evaluations to
ensure effective training.
- Both trainer and trainee document completion of training.
Training resources. Resources for training are available from various sources. Tools for training continue to evolve and
are not limited to traditional methods. Instructional videos, workshops, computer-based programs, and other methods can
be used. The manufacturer's test system instructions and instrument operating manuals should be the primary resource
for information and training in CW sites. Other sources for training on waived testing or specific tests include:
- Manufacturers and distributors who often provide technical assistance, product updates or notifications, and
- Professional organizations that can provide workshops or other training tools.
- State health departments or other government agencies that can provide limited training.
To ensure testing procedures are performed consistently and accurately, periodic evaluation of competency is
recommended, with retraining, as needed, on the basis of results of the competency assessment
(32). Assessment activities should be conducted
in a positive manner with an emphasis on education and promoting good testing practices. Competency can be evaluated
by methods such as observation, evaluating adequacy of documentation, or the introduction of mock specimens by testing
control materials or previously tested patient specimens. External quality assessment or evaluation programs, such as voluntary
PT programs, are another resource for assessment.
Additional Measures to Help Testing Staff Ensure Reliable Results
The CW site director or person overseeing testing should promote quality testing and encourage staff to ask questions and
seek help when they have concerns. Recommendations
Recommended Practices Before Testing
- Identifying a resource person or expert (e.g., a consultant or manufacturer's technical representative), available
either off-site or on-site, to answer questions and be of assistance.
- Posting telephone numbers for manufacturers' technical assistance representatives.
- Designating an appropriately trained person, who understands the responsibilities and impact of changing from one
test system to another, to discuss new products with sales representatives. Uninformed personnel might mistakenly use
a promotional test kit, provided by a distributor or manufacturer's representative, for patient testing without realizing
the consequences of test substitution.
Preparations before performing patient testing are a critical element in producing quality results. Paying attention to
test orders, properly identifying and preparing the patient, collecting a good quality specimen, and setting up the test system
and testing area all contribute to reliable test results.
Test Orders, Patient Identification, and Preparation
Before collecting the specimen, confirm the test(s) ordered and the patient's identification and verify that pretest instructions
or information, as applicable, have been provided. This includes:
- Test orders --- CW sites performing various waived tests should routinely confirm that the written test order is correct.
If there is a question, check with the ordering clinician. Standing orders for certain tests might apply, but they should
- Patient identification --- Identify the patient before collecting the specimen. Because names can be similar and lead
to confusion, use birth dates, middle initials, identification numbers, or other means to ensure the specimen is collected
from the correct patient.
- Pretest instructions --- Some tests require special preparation on the patient's part (e.g., a fasting state for glucose
testing). Provide the patient with pretest instructions, when
appropriate, and when special preparation is needed, verify that
patients received instructions before testing. To
determine if patients followed the instructions, ask them to explain
how they prepared for the test.
- Pretest information --- Discuss factors, test limitations, or medical indications that can affect test results with the
patient, as appropriate, and provide pertinent information such as pamphlets supplied by the test manufacturer, when specified
in the product insert.
Specimen Collection and Handling
The product insert provides details on proper collection, handling, and storage of patient specimens. Collect waived
test specimens exactly as described in the test system instructions, using the appropriate collection device and method to obtain
a quality specimen (33--36). Improperly collected, stored, or compromised specimens should not be tested. Specimens and,
in some cases, test devices need to be appropriately labeled to prevent mix-up.
Waived test specimens. Waived tests are approved for use only with direct, unprocessed specimens that do not
require operator manipulation (Table 8). Specimens that are processed or manipulated by the user (e.g., serum or plasma)
require centrifugation, dilution, extraction, or other preparation steps that require special training or instrumentation and are
not appropriate for waived tests. Sometimes, tests can be performed using both processed and unprocessed specimen types, but
are waived only for the unprocessed specimens, in which case the product insert should identify the appropriate specimen for
the waived test. For example, a single product insert might include instructions for performing a waived test
using unprocessed whole blood and for performing the same test using plasma, which would not be waived. Other examples
include group A streptococcal antigen testing, which is waived only when performed on a throat swab and not when performed on
a microbiology culture, and visual color comparison tests for hCG (pregnancy tests) using urine that are waived, whereas
serum or plasma hCG tests are not waived.
Specimen collection. The person collecting the patient specimen or giving the collection instructions should have
a thorough understanding of the specimen type, proper collection method (including the need to wear gloves or other PPE
as appropriate), and handling to assure a quality specimen
(33--36). Directions for specimen collection, handling, and
storage are included in the product insert and must be followed explicitly. For example, instructions might specify one drop
of capillary blood or include precautions to use the second drop of blood from a fingerstick rather than the first. When gloves
are worn during specimen collection, they should be removed and discarded in an appropriate waste receptacle
before contact with another patient. Hand hygiene should be performed between patients.
Collection devices. Manufacturers might provide or specify specimen collection devices. These devices, whether
supplied with the test system or specified in the product insert, are integral to the test system and should be used to ensure the
correct specimen type and volume to provide reliable results. Containers and collection devices might have additives that affect
the specimen or are part of the test and should not be substituted or altered. For example, throat swab collection kits used
with group A streptococcal antigen tests might look the same; however, they might be made from a variety of fibers or
contain different materials that could interfere with the test or affect organism viability. Whole blood capillary tubes (e.g., used
for cholesterol, hemoglobin A1C, or Helicobacter pylori
testing) can have additives or hold different specimen volumes
which affect test reactions and results.
Fingerstick and venipuncture collection devices are for one-time use only. Never reuse needles, syringes, or lancets. To
avoid transmission of hepatitis B virus, hepatitis C virus, HIV, and other bloodborne pathogens, appropriately discard
sharps, lancets, and platforms for spring-loaded lancets and disinfect instruments contaminated by blood
Specimen labeling. Labeling procedures should meet the needs of the testing site and should be adequate to
prevent specimen mix-up. To prevent errors, always label specimens with pertinent information (e.g., unique patient name or
other unique identifier). Depending on workflow, specimen labeling also might include the date and time of collection
and identification of the collector. For waived tests in which the specimen is applied directly to the test device (e.g., throat
swabs for group A streptococcal antigen), the test strip, cassette, or other device should be labeled with the patient
identification before collecting the specimen, especially if more than one test is being performed at the same time.
Preparing the Testing Area, Test Materials, and Equipment
Preparing the testing area and materials (e.g., kits, reagents, control materials, and equipment) before testing
patient specimens is essential to maintaining efficient workflow and good quality testing
(Table 9). Before beginning the test, read and understand the test instructions specified in the product
insert and included in the CW site's procedures. Verify that
the instructions are current for the test in use and that no changes have been made. Do not use product inserts that are out of
date for the test system currently in use. When opening a new kit, check for notifications in the external labeling or special
notices that might be included with product inserts or packaging.
Additional considerations for good testing practices are:
Recommended Practices During Testing
- Abide by expiration dates and discard expired reagents and test kits as soon as the expiration date elapses.
- When preparing to perform testing, allow time for any refrigerated items, including reagents or patient specimens,
to reach room temperature before testing, if specified in the product insert.
When the testing area is prepared and the specimen has been collected, the process continues to the testing phase.
Important activities during this phase include QC testing, test performance, result interpretation and recording.
Quality Control Testing
Performing QC testing procedures provides assurance that the test performs as expected and alerts the user when
problems occur. QC testing is designed to detect problems that might arise because of operator error, reagent or test kit
deterioration, instrument malfunction, or improper environmental conditions. Test procedures should describe the type of controls to
be used, how to perform QC testing (including QC testing frequency), and actions to be taken when QC results
Types of controls. Two types of controls typically found in waived tests are:
- Internal, procedural, or built-in controls --- evaluate whether certain aspects of the test system are working properly.
They are designed to verify that the test system is working as expected, that sufficient specimen was added and, for unitized
test devices, whether it migrated through the test strip properly. Certain test systems might have electronic internal controls
to monitor electronic functions.
- External controls --- mimic patient specimens and monitor the testing process, from specimen application
to result interpretation, to assure proper test performance. They might be provided as liquid or other materials similar
to patient specimens and might be included with the test system or purchased separately.
Frequency of control testing. For certain test systems, the product insert describes the minimum conditions
or recommended frequencies for testing internal and/or external controls. Each site should determine the appropriate
control testing frequency for each test system and the frequency should not be less than specified in the product insert.
When determining the frequency for running external controls, consider the robustness of the test, stability of the environment,
and skills and knowledge of the testing personnel. At a minimum, external controls should be tested with each new shipment
of utilized test devices, when testing a new lot number, and by each new operator before conducting testing. Controls should
be tested either before or concurrent with patient specimens by the same personnel who routinely perform patient testing.
Corrective action when control testing fails. If controls do not perform as expected, patient testing should not
be performed or results reported until the problem is identified and corrected. The product insert should provide information
on procedures for handling unexpected control results, identifying sources of error (including interfering substances),
and manufacturer contact information for technical assistance. This information might be incorporated into the
facility's procedures or posted for quick reference. The test site should have telephone numbers or other contact information
readily available (e.g., numbers for manufacturers' technical assistance, the facility's director, consultant, or public
Documentation. Documenting and monitoring control testing results provides an indication that the test was
properly performed by the operator and the test system (reagents, instruments, or any components) performed as expected. Records
of control results should be periodically reviewed to detect shifts or changes in performance over time.
Performing the Test
The following points are important to remember when performing the test:
- Follow the steps in the test procedure in the exact order described in the product insert.
- Test controls at the frequency determined by the CW site.
- Pay attention to timing for waived tests, particularly unitized test devices that must be read during specific time
intervals. Incorrect timing of these types of tests can give erroneous test results. Insufficient timing can result in false negative
or invalid results because the specimen might not react completely with test system reagents. Time
intervals longer than those specified in the product insert can result in false positive, false negative, or invalid
results because of exaggerated color development, fading of reaction products, or migration beyond a visible range. Therefore, it is important to have a
system established to read results during the correct timeframe, especially if conducting more than one test at a time.
Suggestions for helping to ensure correct timing of tests include using timers that beep until turned off, using timers that can easily
be worn or attached to clothing, using multiple timers when performing more than one test at a time, and maintaining
extra timers and batteries.
Test Results Interpretation
When the test is complete, interpret the results according to instructions in the product insert (including the quick
reference guide). Test results are of the following two types:
- Quantitative --- Tests that provide numerical results generated by the test device or instrument. Numerical results
are values corresponding to the concentration of the specific substance being measured. The value includes
specific measurement units (e.g., such as a glucose result of 100 mg/dL). No interpretation is necessary to read the result.
- Qualitative --- Tests that detect whether a particular substance, condition, or microbiological organism is present
or absent. Results are interpreted as positive/reactive, negative/nonreactive, or invalid. Invalid results might indicate
a problem with the specimen or the test system. Diagrams, color photographs, and color-comparison charts are often
part of the product insert and quick references and serve as guides for interpretation.
If a discrepancy is identified between the patient's test
results and the clinical information or if the results are invalid
or otherwise compromised, testing should be repeated.
Results should not be reported until the problem is resolved. Follow
the steps in the product insert to resolve problems with test results. Unitized test system instructions usually suggest repeating
the test with a new device and referring to QC or trouble-shooting procedures. If repeat testing does not resolve the
problem, contact the manufacturer or product technical representative. Quantitative results can be obtained that are beyond
measuring range of the instrument or test device. Each site should have documentation of quantitative test measuring
ranges and a procedure for handling test results that are beyond the reportable ranges, either low or high.
Record test results according to the site's policy. Results can be recorded directly in a patient's chart, in log books, or on
a separate report form. Records or logs of test results should have enough detail so the test site can retrieve
information. Quantitative results should be recorded using the units of measurement of the test system. Qualitative test results should
be recorded using interpretive words or abbreviations such as positive, negative, reactive or R, or nonreactive or NR instead
of symbols like plus and minus (+, -) to help avoid clerical errors because a negative (-) sign can easily be changed to a
positive (+) sign. If a test result is not acceptable or requires repeat testing (e.g., out of range or invalid), record the initial result,
noting it was unacceptable, take steps necessary to
resolve the problem, then record the correct result. Good laboratory
practices include recording what happens, whether
acceptable or not, and what is done to correct problems
encountered during testing.
Recommended Practices After Testing
After-testing activities include issuing test reports, supplemental or confirmatory testing, public health disease reporting
(if required), testing area cleanup, biohazard waste disposal, and documentation of testing activities.
After the completion of the test, results are documented and reported. Patient reports should be legible and reported in
a timely manner to the appropriate person. Reports should meet the needs of the testing site and should be
appropriately standardized so reports generated on-site are easily distinguishable from referral laboratory reports. Verbal reports of test
results should be documented and followed by a written
report. Waived testing sites, such as point-of-care sites or physicians'
offices, might accurately and legibly record results directly in the patient's record as a matter of practice. If results are not
recorded directly in a patient's chart, they should be recorded in a written report format that includes all information needed
to correctly identify and interpret the results as determined by the testing site
Critical values are test results necessary for patient evaluation or treatment that require immediate notification to
the clinician. Each site should define the critical values, if appropriate, for the tests in use and ensure that testing personnel
are aware of these values and the procedure for alerting the clinician. Procedures should be in place to ensure documentation
of critical values and timely notification of the proper medical personnel.
Supplemental or Confirmatory Testing
The product insert should explain when supplemental testing is needed to confirm a waived test result or when the test is
to be used as part of a multitest algorithm. A confirmatory test could be a different waived test (performed at the testing site
or another CW site) or a nonwaived test performed by a CLIA-certified referral laboratory
(37) (Table 11). When nonwaived confirmatory testing is needed, the patient can be sent to another facility for specimen collection and testing, or the
specimen can be collected at the CW site and sent to a referral laboratory.
The CW site should have written policies to ensure confirmatory and supplemental testing is performed when needed.
For each waived test that requires additional testing, the CW site should document the processes and procedures necessary
to manage referral or confirmatory testing. When a CW site collects specimens for referral, procedures should include
- Instructions for ordering additional tests, contact information for the referral laboratory used, and examples of
completed test request forms.
- Specimen collection and labeling procedures with
examples of forms used to track referred specimens.
- Safe specimen transport or shipping information as necessary, including special packaging and shipping requirements
for confirmatory or supplemental tests for infectious diseases (e.g., HIV).
Maintaining records of referred testing is important for
patient care and follow-up. Logs and other records should
have sufficient information to track and retrieve the test
results and reports, such as:
- Information linking the referred specimen to patient
- The name and contact information for the referral
- The test name and date referred,
- Complete test results and the date received, and
- The date the final report is issued.
Public Health Reporting
Federal and state public health agencies require testing
facilities to report confirmed positive results for certain
infectious diseases (e.g., HIV, influenza, and Lyme disease)
(38,39). Testing facilities should confer with local public health agencies
for the most current information on required reporting procedures since diseases identified for reporting can change over
time, and state requirements might vary.
Biohazard Waste Disposal
Dispose of the biohazardous waste generated in specimen collection and testing according to site procedures that need to
be in compliance with local ordinances, state, and federal OSHA regulations as previously discussed.
Documents and Records
Documentation is essential to assure quality waived testing. Proper documentation is necessary for monitoring and
assessing test performance, identifying and resolving problems that could affect patient testing, retrieving and verifying
information, and maintaining adequate patient and personnel records. Log books or electronic systems can be used for maintaining
and tracking information. In some cases, records might be part of the patient's medical chart. Testing records should be
maintained in chronological order to facilitate retrieval of
information if needed. In addition, control records should be kept in the
order in which they were completed so they can easily be compared with test records if there are questions about testing
performed within a specific time period. The person responsible for testing oversight and decision-making should review
records periodically. State regulations or other governmental agencies might require CW sites to retain documents and records for
a specific length of time.
Aspects of testing for which records or documentation are recommended include:
- Test orders
- Test procedures or work instructions (e.g., written procedures specific to the CW site and current product inserts)
- Records of testing materials used, test system and equipment function checks, and maintenance
--- Daily records of temperatures for refrigerators, freezers, and the testing area, as needed for the tests performed
--- Lot numbers, dates used, and expiration dates of test systems and reagents
--- Date and time (if applicable) of equipment function checks and any maintenance performed
--- As applicable, notifications from manufacturers about product recalls or other problems, especially if the recalls or
warnings refer to specific lot numbers or test systems
- Test results, including any confirmatory or supplemental testing
- QC testing results and corrective action taken if control results are unacceptable
--- Date and time (if applicable) of control testing
--- Lot number and expiration date of external controls
- Records of any test system failures, troubleshooting, and corrective action taken when problems are
identified, including related communication with testing personnel
- Personnel training and competency assessment
- Records of PT or other external quality assessment
Good laboratory practices can be expanded to include
assessment activities to evaluate and improve the quality of CW
site testing. Assessment activities can be either internal or external, depending on the needs, resources, and practices of the site.
Objective internal assessment offers flexible, low-cost
options for evaluating quality such as self-conducted
inspections, supervisory review of documented problems that occur in the different phases of the testing process, review of
documentation, and testing and reporting procedures. Test performance can be assessed, if specimens are suitable,
by exchanging specimens with another testing facility using the same test method(s) and comparing the results. Results
from these assessment activities should be documented and evaluated, noting any irregularities and the actions taken to
resolve problems or improve processes or procedures.
Because CW sites are not routinely inspected by CMS, voluntary inspections by peers or consultants can offer
additional educational opportunities and feedback on current practices along with ideas for quality improvement. Voluntary
external inspections evaluate the testing site practices and documentation systems, and a more narrowly focused assessment of
test performance can be accomplished by participating in performance evaluation programs or subscribing to PT programs.
These programs provide challenge samples to test as if they were patient specimens and the results are evaluated with respect to
how close they are to the intended target values. Participation in these types of programs can be used to evaluate overall
testing performance and as a training or educational tool for testing personnel.
This report summarizes the findings of multiple surveys of sites performing waived testing throughout the United
States. Although the surveys were conducted through several mechanisms, the findings lead to similar conclusions about lapses
in quality in CW sites, and they highlight the need for additional education and training related to waived testing for CW
site directors and testing personnel. The recommendations provided in this report are intended to serve as a guide to improve
the quality of testing in CW sites and enhance patient
safety. They can be disseminated by a variety of individuals
and organizations and adapted for use in different settings where waived testing is conducted. Continued surveillance
and monitoring of waived testing performance is needed to determine the effectiveness of these recommendations on
protecting and improving the public's health.
The preparers acknowledge the contributions and assistance provided by John Hancock, James Handsfield, MPH, and
Rhonda Whalen, MS, of the Division of Public Health Partnerships, National Center for Health Marketing, Coordinating Center for
Health Information and Service, CDC; Daralyn Hassan, MS, and the CMS Waived Laboratory Project Team, Division of Laboratory
Services, Survey and Certification Group, Center for Medicare and State Operations, CMS.
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Terms and Abbreviations Used in This Report
true or target value; freedom from error;
the accuracy of results can be measured by comparing them to
results accepted as correct (e.g., standard methods), or by
comparing them with those from another laboratory that uses a
a substance or constituent for which a
laboratory conducts testing
a protein formed in the body in response to
a foreign substance (e.g., bacteria, viruses or chemical toxins)
and that interacts with the foreign substance to weaken or
any substance that, when introduced into
the body, causes the development of an immune response, such as
Arkansas Sentinel Network
a biological agent that has the capacity to
produce deleterious effects on humans, such as microorganisms
waste containing pathogens with sufficient
virulence and quantity so that exposure to the waste by a
susceptible host could result in an infectious disease
the application of combinations of
laboratory practice and procedure, laboratory facilities, and
safety equipment when working with potentially infectious
microorganisms to prevent infection
microorganisms that, when present in human
blood, can cause disease in humans. These pathogens include, but
are not limited to, hepatitis B virus, hepatitis C virus, and
human immunodeficiency virus (HIV)
the process of testing and adjusting an
instrument or test system to provide a known relationship
between the value of the substance being measured by the test
and the test systemís measurement response. A calibration check
is a mechanism to be sure the test system has remained stable
and the results remain accurate
a process of separating blood or other body
fluid cells from liquid components using a device (centrifuge)
containing compartments that spin rapidly around a central axis
Clinical Laboratory Improvement Amendments of 1988
Clinical Laboratory Improvement Advisory
Clinical and Laboratory Standards Institute
Centers for Medicare & Medicaid Services
evaluation of a personís ability to perform
a test and to use a testing device; this includes all aspects of
testing, from specimen collection to result reporting
an additional more specific test performed
to rule out or confirm a preliminary test result to provide a
a device or solution used to monitor a test
system to ensure proper test performance and correct results
test results that require immediate
notification to the clinician for patient evaluation or
Certificate of Waiver
CW testing site
the location where waived testing takes
place; a facility holding a CW
a test that identifies a disease or
direct microscopic examination
the direct examination of a patient
specimen using a microscope
control materials that mimic patient
specimens and monitor the testing process from specimen
application to result interpretation
Food and Drug Administration
FDA Modernization Act
United States Department of Health and
Health Insurance Portability and
Accountability Act of 1996
human immunodeficiency virus
procedural or built-in controls; controls
that are built into a testing device and designed to verify that
the test system is working as expected
a packaged set containing test devices,
instructions, reagents, and supplies needed to perform a test
and generate results
Laboratory Medicine Sentinel Monitoring
nonreactive or NR
a result that indicates the absence of the
constituent that the test is designed to detect
complex tests that do not meet the CLIA
criteria for waiver and require training and specific quality
measures to ensure the accuracy and reliability of test results
New York Sentinel Network
Department of Health and Human Services
Office of Inspector General
Occupational Safety and Health
the liquid portion of anticoagulated blood
that does not contain cells. If a chemical agent or
anticoagulant is added to a blood specimen to prevent clotting,
the specimen can be separated by centrifugation into cells and
Pacific Northwest Sentinel Network
physician office laboratory
personal protective equipment; specialized
clothing or equipment worn by an employee for protection against
provider-performed microscopy procedures; a
subcategory of moderate complexity testing under CLIA
reproducibility; the measure of the
closeness of the results obtained when analyzing the same sample
more than once; the measure of agreement between replicate
measurements of the same material
a handbook that contains test methods and
other information needed to perform testing
written product information usually
supplied by the manufacturer with each test kit or test system
containing instructions and critical details for performing the
test; also referred to as package insert
proficiency testing; an external quality
assessment program in which samples are periodically sent to
testing sites for analysis
a test that detects whether a particular
analyte, constituent, or condition is present or absent
a group of activities to monitor and
evaluate the CW siteís entire testing process to help ensure
that test results are reliable, improve the testing process, and
promote good quality testing practices
quality control; the procedures used to
detect and correct errors that occur because of test system
failure, adverse environmental conditions and variance in
operator performance, as well as the monitoring of the accuracy
and precision of the test performance over time
a test that measures the concentration or
amount of an analyte in a specimen, whose results are expressed
quick reference instructions
cards or small signs containing diagrams or
flow charts with essential steps for conducting a test that are
often included with waived test systems
reactive or R
a result that indicates the presence of the
constituent that the test is designed to detect
a substance that produces a chemical or
biological reaction with a patient specimen that allows
detection or measurement of the analyte for which the test is
the range of test values expected for a
designated population of persons (e.g., 95% of persons presumed
to be healthy [or normal])
a laboratory that receives specimens from
CW sites to perform additional testing, often for follow-up
confirmatory testing; the majority of referral laboratories
perform nonwaived testing
the span of test result values for which
the instrument or test device can accurately measure
the lowest concentration of an analyte that
can reliably be detected or measured by a test system
the cell-free liquid remaining after whole
blood has clotted or coagulated
the ability of a test to detect a
particular substance or constituent without interference or
false reactions by other substances
an approach used in healt-care settings to
reduce the risk for transmission of microorganisms from both
recognized and unrecognized sources of infection in a wide
variety of human sources. The nature of medical procedures and
testing in these settings requires expansion of Universal
Precautions to include feces, nasal secretions, saliva, sputum,
sweat, tears, urine, and vomitus, even when no visible blood is
the state health agency or other
appropriate state or local agency that has an agreement under
Section 1864 of the Social Security Act and is used by CMS to
perform surveys and inspections
the instructions and all of the
instrumentation, reagents, and supplies needed to perform a test
and generate results
total testing process
series of activities or path of workflow
for performing testing that can be divided into three major
phases; before testing, during testing, and after testing
unitized test device
a self-contained test device to which a
specimen is added directly and in which all steps of the testing
process occur. A unitized device is used for a single test and
must be discarded after testing.
an approach to controlling infection.
According to the concept of Universal Precautions, all human
blood and certain human body fluids are treated as if known to
be infectious for HIV, hepatitis B virus, hepatitis C virus, and
other bloodborne pathogens.
a test system, assay, or examination that
has been cleared by the FDA for home use, or HHS has determined
meets the CLIA criteria of being a simple test with an
insignificant risk for an erroneous result
blood containing all its cellular
components that has not undergone centrifugation or had the
Clinical Laboratory Improvement Advisory Committee Workgroup
Chair: Jared N. Schwartz, MD, Department of Pathology and Laboratory Medicine, Presbyterian Healthcare, Charlotte, North Carolina.
Co-Chair: Kathryn M. Foucar, MD, Department of Pathology, University of New Mexico, Albuquerque, New Mexico.
Members: Jennifer M. Alfisi, JD, Health Industry Distributors Association, Alexandria, Virginia; Kimberle C. Chapin, MD, Department of
Pathology, Rhode Island Hospital, Providence, Rhode Island; Mary Beth Clark, Emory Healthcare, Atlanta, Georgia; Martha H. Crenshaw, MD, Stone
Mountain, Georgia; Jacinto Del Mazo, MD, Del Mazo Medical Services, Atlanta, Georgia; Paula W. Garrott, EdM, Clinical Laboratory Science
Department, University of Illinois at Springfield, Illinois; Barbara M. Goldsmith, PhD, Caritas St. Elizabeth's Medical Center, Boston, Massachusetts; Luann
Ochs, MS, Roche Diagnostics Corporation, Indianapolis, Indiana; Barbara E. Robinson-Dunn, PhD, William Beaumont Hospital, Royal Oak, Michigan;
Lou F. Turner, DrPH, North Carolina State Laboratory of Public Health, Raleigh; Robin Weiner, Biosite Inc., San Diego, California; Thomas
L.Williams, MD, Methodist Pathology Center, Nebraska Methodist Hospital, Omaha.
Clinical Laboratory Improvement Advisory Committee
Chair: SUNDWALL, David N. Sundwall, MD, Utah State Health Department, Salt Lake City, Utah.
Executive Secretary: Robert Martin, DrPH, National Center for Health Marketing, CDC, Atlanta, Georgia.
Members: Kimberle C. Chapin, MD, Department of Pathology, Rhode Island Hospital, Providence, Rhode Island; Joeline D. Davidson, MBA,
Georgia Health System, LaGrange, Georgia; Kathryn M. Foucar, MD, Department of Pathology, University of New Mexico, Albuquerque; Paula
W. Garrott, EdM, Clinical Laboratory Science Dept, University of Illinois at Springfield; Patrick A. Keenan, MD, Department Family Medicine
and Community Health, University of Minnesota, Minneapolis; Michael Laposata, MD, Massachusetts General Hospital, Boston; Margaret
Mary McGovern, MD, Molecular Genetics Laboratory, Mount Sinai School of Medicine, Mount Sinai Medical Center, New York, New York; Dina R.
Mody, MD, The Methodist Hospital, Houston, Texas; Valerie L. Ng, MD, Alameda County Medical Center/Highland Hospital Clinical Laboratory,
Oakland, California; Peter J. Gomatos, MD, Fort Lauderdale, Florida; Cyril Michael Hetsko, MD, Madison, Wisconsin; Anthony N. Hui, MD,
Northwest Arkansas Pathology Associates, Fayetteville, Arkansas; Kevin P. Kandalaft, Provider Contracting & Provider Services Lovelace Health Systems,
Inc., Albuquerque, New Mexico; Barbara E. Robinson-Dunn, PhD, William Beaumont Hospital, Royal Oak, Michigan; Jared N. Schwartz,
MD, Department of Pathology and Laboratory Medicine, Presbyterian Healthcare, Charlotte, North Carolina; Albert H. Stahmer, Golden, Colorado; Lou
F. Turner, DrPH, North Carolina State Laboratory of Public Health, Raleigh; Thomas L. Williams, MD, Methodist Pathology Center, Nebraska
Methodist Hospital, Omaha; Jean Amos Wilson, PhD, Focus Diagnostics, Inc., Cypress, California.
Ex Officio Representatives: Steven I. Gutman, MD, Office of In Vitro Diagnostic Device Evaluation & Safety, Food and Drug
Administration, Washington, DC; Thomas L. Hearn, MD, National Center for Health Marketing, CDC, Atlanta, Georgia; Judith Yost, MA, Division
Laboratories Services, Center for Medicaid and State Operations, Centers for Medicare & Medicaid Services.
Liaison Representative: Luann Ochs, MS, Roche Diagnostics Corporation, Indianapolis, Indiana.
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Date last reviewed: 10/26/2005