Current through August 26, 2024
(1) LABORATORY
APPROVED.
(a) The department may approve a
laboratory to perform a drug residue test as a screening test, even though the
laboratory is not certified under s.
ATCP 77.03 to perform the test as a confirmatory test. An
approval expires on December 31 of each year. An approved laboratory shall
comply with s.
ATCP 65.76(2)
(b).
(b) The department may not approve a
laboratory under par. (a) unless all of the following apply:
1. The department has approved at least one
individual under sub. (2) to perform the drug residue screening test at the
approved laboratory.
2. The
laboratory has written agreements with one or more certified laboratories to
provide the confirmatory testing required under s.
ATCP 65.76(2) (b)
3.
(c) The department shall inspect a laboratory
under par. (a) before approving the laboratory to perform a visual read drug
residue screening test, and before approving any individual under sub. (2) to
perform a visual read drug residue screening test at that
laboratory.
(2) ANALYSTS
APPROVED.
(a) No individual may perform a
drug residue screening test unless the department approves that individual to
perform that test at a laboratory approved under sub. (1).
(b) Before the department approves an
individual under par. (a) to perform a visual read test, the department shall
perform an on-site competency evaluation under sub. (4).
(c) The department's approval under par. (a)
expires on December 31 of each year unless, by that date, the laboratory
operator attests to the department that the individual has successfully
completed an annual proficiency evaluation under sub. (5).
(d) The department may suspend or revoke an
approval under par. (a) for cause.
(3) APPROVAL FEES. A laboratory operator
shall pay the following fees to acquire and maintain a laboratory approval
under sub. (1):
(a) An initial fee of $732,
except as provided in par. (b) or (c).
(b) An initial fee of $180 if the laboratory
tests milk for only one dairy plant operator and all the following apply:
1. The dairy plant operator receives only
grade B milk.
2. The dairy plant
operator receives milk from not more than 5 producers.
3. The dairy plant operator receives not more
than 10,000 lbs. of raw milk per week.
(c) An initial fee of $72 if the laboratory
does not apply for approval to perform any visual read test.
(d) A fee of $36 for each individual, in
excess of 3 individuals, that the department evaluates under sub. (4) at the
time of the initial laboratory inspection under sub. (1)(c).
(e) An annual renewal fee of $72 for each
annual renewal of the laboratory approval, except that the renewal fee is $36
if the laboratory qualifies under par. (b).
(f) A fee of $180 for each laboratory visit,
other than the initial inspection under sub. (1) (c), that the department makes
for the purpose of evaluating individuals under sub. (4). This single fee of
$180 covers all of the individual evaluations performed during the department's
visit, regardless of the number of individuals evaluated.
(4) COMPETENCY EVALUATION. Before the
department approves an individual to perform a visual read test, the department
shall observe and evaluate that individual's competency to perform that test.
The department shall use an appropriate FDA 2400 series form to conduct the
evaluation.
Note: FDA 2400 series forms are on file with
the department, the secretary of state and the legislative reference
bureau.
(5) ANNUAL
PROFICIENCY EVALUATION.
(a) An individual
approved to perform a drug residue screening test shall complete an annual
proficiency evaluation. An evaluator approved by the department shall
administer the annual proficiency evaluation. The department may approve the
laboratory operator to serve as evaluator, except that an independent evaluator
shall administer annual proficiency evaluations for analysts performing visual
read tests. The evaluator shall report the results of each proficiency
evaluation to the department within 7 days after the evaluation is
completed.
(b) In a proficiency
evaluation, the evaluated individual shall examine the number of samples
required under either par. (d) or (e). The evaluator may prepare the samples
used in proficiency evaluations, except for samples used in a visual read
proficiency test. The contents of the samples shall be known only to the
evaluator, and not to the evaluated individual. The evaluator shall evaluate
the individual's proficiency by comparing the individual's results to the known
contents of the samples, and shall report those results to the
department.
(c) A proficiency
evaluation under par. (a) shall be conducted according to a standard evaluation
procedure that the department approves in writing. A standard evaluation
procedure shall comply with this subsection and shall include standards for all
the following:
1. The evaluator's preparation
of proficiency evaluation samples.
2. The analyst's examination of proficiency
evaluation samples.
3. Deadlines
for examining proficiency evaluation samples and reporting test
results.
4. The evaluator's review
and rating of the individual's proficiency.
(d) For a drug residue screening test other
than a visual read test, a proficiency evaluation under par. (a) shall include
3 samples. To pass the proficiency evaluation, the individual shall interpret
all 3 sample results correctly.
(e)
For a visual read test, a proficiency evaluation under par. (a) shall include
at least 6 but not more than 20 samples. To pass a proficiency evaluation
involving 6 to 10 samples, an individual shall interpret no more than one
sample result incorrectly. To pass a proficiency evaluation involving 11 to 20
samples, an individual shall interpret no more than 2 sample results
incorrectly.
(6) FAILED
PROFICIENCY EVALUATION; LOSS OF APPROVAL.
(a)
If an individual approved to perform a drug residue screening test fails his or
her first annual proficiency evaluation related to that test, the individual is
no longer approved to perform that test.
(b) If an individual approved to perform a
drug residue screening test passes his or her first annual proficiency
evaluation related to that test, but subsequently fails 2 consecutive annual
proficiency evaluations, the individual is no longer approved to perform that
test.
(c) The department may
restore an approval lost under par. (a) or (b) if the individual completes a
training program approved by the department and passes an on-site competency
evaluation under sub. (4). If the individual subsequently fails his or her
first annual proficiency evaluation related to the drug residue screening test,
the individual may no longer perform that test. The department may again
restore the approval if the individual again meets the restoration requirements
under this paragraph.
(7)
LIST OF APPROVED ANALYSTS. The department shall maintain, for each laboratory
approved under sub. (1), a list of individuals currently approved to perform
drug residue screening tests at that laboratory. The list shall identify the
drug residue screening tests that each individual is approved to
perform.
(8) NOTICE OF STAFFING
CHANGES.
(a) A laboratory operator shall
notify the department within 30 days after any of the following occurs:
1. An individual approved under sub. (2)
leaves employment with that laboratory.
2. There is a change in the name of any
individual approved under sub. (2).
(b) A laboratory operator shall notify the
department within 7 days after a staffing change if, as a result of that
change, the laboratory has no individuals approved under sub. (2) to perform a
drug residue screening test that the laboratory is authorized to
perform.