Current through Register Vol. 41, No. 3, September 23, 2024
A. The
standards for on-site assessment are found in Volume 2, Module 3 of the TNI
standards. The requirements specific to environmental laboratories are set out
in this section.
B. DCLS shall
conduct a comprehensive on-site assessment of an environmental laboratory prior
to granting final primary accreditation to the laboratory.
C. Frequency of on-site assessment.
1. DCLS shall reassess each accredited
laboratory every two years starting from the date of the previous assessment
plus or minus six months.
2. Other
on-site assessments.
a. If DCLS identified a
deficiency on a previous on-site assessment, the agency may conduct a follow-up
on-site assessment.
b. DCLS may
conduct an on-site assessment under the following circumstances:
(1) A laboratory applies to modify its scope
of accreditation;
(2) A transfer of
ownership occurs that affects personnel, equipment, or the laboratory
facilities; or
(3) A laboratory
applies for an exemption or a variance.
c. Any other change occurring in a
laboratory's operations that might reasonably be expected to alter or impair
analytical capability and quality may trigger an on-site assessment.
D. Announced and
unannounced on-site assessments. DCLS, at its discretion, may conduct either
announced or unannounced on-site assessments. Advance notice of an assessment
shall not be necessary.
E.
Preparation for the on-site assessment.
1.
Prior to the actual site visit, DCLS may request in writing from a laboratory
those records required to be maintained by this chapter.
2. DCLS may opt not to proceed with an
on-site assessment based on nonconformities found during document and record
review.
F. Areas to be
assessed.
1. DCLS shall assess the laboratory
against the standards incorporated by reference and specified in
1VAC30-46-200
and
1VAC30-46-210.
2. The laboratory shall ensure that its
quality manual, analytical methods, quality control data, proficiency test
data, laboratory SOPs, and all records needed to verify compliance with the
standards specified in
1VAC30-46-200
and
1VAC30-46-210
are available for review during the on-site assessment.
G. National security considerations.
1. Assessments at facilities owned or
operated by federal agencies or contractors may require security clearances,
appropriate badging, or a security briefing before the assessment
begins.
2. The laboratory shall
notify DCLS in writing of any information that is controlled for national
security reasons and cannot be released to the public.
H. Arrival, admittance, and opening
conference.
1. Arrival. DCLS and the
laboratory shall agree to the date and schedule for announced on-site
assessments.
2. Admittance of
assessment personnel. A laboratory's refusal to admit the assessment personnel
for an on-site assessment shall result in an automatic failure of the
laboratory to receive accreditation or loss of an existing accreditation by the
laboratory, unless there are extenuating circumstances that are accepted and
documented by DCLS.
3. Health and
safety. Under no circumstance, and especially as a precondition to gain access
to a laboratory, shall assessment personnel be required or even allowed to sign
any waiver of responsibility on the part of the laboratory for injuries
incurred during an assessment.
4.
Opening conference. An opening conference shall be conducted and shall address
the following topics:
a. The purpose of the
assessment;
b. The identification
of assessment personnel;
c. The
test methods that will be examined;
d. Any pertinent records and procedures to be
examined during the assessment and the names of the individuals in the
laboratory responsible for providing assessment personnel with such
records;
e. The roles and
responsibilities of laboratory staff and managers;
f. Any special safety procedures that the
laboratory may think necessary for the protection of assessment
personnel;
g. The standards and
criteria that will be used in judging the adequacy of the laboratory
operation;
h. Confirmation of the
tentative time for the exit conference; and
i. Discussion of any questions the laboratory
may have about the assessment process.
I. On-site laboratory records review and
collection.
1. Records shall be reviewed by
assessment personnel for accuracy, completeness, and the use of proper
methodology for each analyte and test method to be evaluated.
2. Records required to be maintained pursuant
to this chapter shall be examined as part of an assessment for
accreditation.
J.
Observations of and interviews with laboratory personnel.
1. As an element of the assessment process,
the assessment team shall evaluate an analysis regimen by requesting that the
analyst normally conducting the procedure give a step-by-step description of
exactly what is done and what equipment and supplies are needed to complete the
regimen. Any deficiencies shall be noted and discussed with the analyst. In
addition, the deficiencies shall be discussed in the closing
conference.
2. Assessment personnel
may conduct interviews with appropriate laboratory personnel.
3. Calculations, data transfers, calibration
procedures, quality control, and quality assurance practices, adherence to test
methods, and report preparation shall be assessed for the complete scope of
accreditation with appropriate laboratory analysts.
K. Closing conference.
1. Assessment personnel shall meet with
representatives of the laboratory following the assessment for a closing
conference.
2. During the closing
conference, assessment personnel shall inform the laboratory of the preliminary
findings and the basis for such findings. The laboratory shall have an
opportunity to provide further explanation or clarification relevant to the
preliminary findings. If the laboratory objects to the preliminary findings
during the closing conference, all objections shall be documented by the
assessment personnel and included in the final report to DCLS.
3. Additional problem areas may be identified
in the final report.
L.
Follow-up and reporting procedures.
1. DCLS
shall provide an on-site assessment report to the laboratory documenting any
deficiencies found by DCLS within 30 calendar days of the last day of the
on-site assessment.
2. When
deficiencies are identified in the assessment report, the laboratory shall have
30 calendar days from the date of its receipt of the on-site assessment report
to provide a corrective action plan to DCLS.
3. The laboratory's corrective action plan
shall include the following:
a. Any objections
that the laboratory has with regard to the on-site assessment report;
b. The action that the laboratory proposes to
correct each deficiency identified in the assessment report;
c. The time period required to accomplish the
corrective action; and
d.
Documentation of corrective action that the laboratory has already completed at
the time the corrective action plan is submitted.
4. If the corrective action plan, or a
portion of the plan, is determined to be unacceptable to remedy the deficiency,
DCLS shall provide written notification to the responsible official and
technical manager of the laboratory, including a detailed explanation of the
basis for such determination. Following receipt of such notification, the
laboratory shall have an additional 30 calendar days to submit a revised
corrective action plan acceptable to DCLS.
5. DCLS may suspend accreditation from a
laboratory under
1VAC30-46-95
B 3 or withdraw accreditation from a laboratory under
1VAC30-46-100
B 5 if DCLS finds the second revised corrective action plan to be
unacceptable.
6. The laboratory
shall submit documentation to DCLS that the corrective action set out in its
plan has been completed within the time period specified in the plan.
7. DCLS, under
1VAC30-46-100
B 6, may withdraw accreditation from a laboratory if the laboratory fails to
implement the corrective actions set out in its corrective action
plan.
8. DCLS shall grant final
accreditation as specified in
1VAC30-46-70
K upon successful completion of any required corrective action following the
on-site assessment.
Statutory Authority: § 2.2-1105 of the Code of
Virginia.