ATCP 77.22(3)(a)(a) Before the department certifies an analyst to perform any test listed under s. ATCP 77.02 (1) or (2), the department shall observe and evaluate that analyst’s competency to perform that test. ATCP 77.22(3)(b)(b) Whenever the department performs a mandatory inspection of a laboratory under s. ATCP 77.14 (1), the department shall perform a competency evaluation under par. (a) of every analyst who performs a test listed under s. ATCP 77.02 (1) or (2). ATCP 77.22(3)(c)(c) The department shall use an appropriate FDA 2400 series form or if no FDA 2400 series form applies, another standard form to evaluate an analyst’s competency under par. (a). If an analyst performs plate loop counts, electronic bacteria counts, or electronic somatic cell counts, the department shall check the analyst’s accuracy based on any statistical comparisons required by those tests. ATCP 77.22(4)(4) Annual proficiency evaluation. An analyst who performs a test listed under s. ATCP 77.02 (1) or (2) shall complete an annual proficiency evaluation for that test if an annual proficiency evaluation is required under s. ATCP 77.24. ATCP 77.22(5)(5) Conditional certification. If the department determines under sub. (3) that an analyst is competent to perform a test, but the analyst has not yet completed a proficiency evaluation under s. ATCP 77.24 for that test, the department shall conditionally certify the analyst. If a conditionally certified analyst fails a proficiency evaluation under s. ATCP 77.24, the department shall summarily suspend the analyst’s certification to perform that test. ATCP 77.22(6)(6) Full certification. If the department determines under sub. (3) that an analyst is competent to perform a test, and the analyst also passes a proficiency evaluation under s. ATCP 77.24 for that test, the department shall fully certify that analyst to perform that test. ATCP 77.22(7)(7) Provisional certification and restoration of full certification. ATCP 77.22(7)(am)(am) An analyst shall be placed in provisional certification if one of the following occurs: ATCP 77.22(7)(am)1.1. If a fully certified analyst fails a proficiency evaluation under s. ATCP 77.24 for any test, the department shall issue a notice stating that the analyst is provisionally certified to perform that test. ATCP 77.22(7)(am)2.2. If the department conducts a biennial inspection of a laboratory under s. ATCP 77.14 (1) and a fully certified analyst is not present to demonstrate competence to perform the test(s) they are certified for, the department shall issue a laboratory report stating that the analyst is provisionally certified to perform that test. ATCP 77.22(7)(c)(c) If an analyst is provisionally certified because of failing a proficiency evaluation under s. ATCP 77.24 and that analyst passes a proficiency evaluation under s. ATCP 77.24 on a new set of proficiency samples, the department shall restore the analyst to full certification. ATCP 77.22(7)(d)(d) If an analyst is provisionally certified because they were not present to demonstrate their competence to perform the tests they are certified for during the biennial inspection of the laboratory, they shall remain in provisional certification status until they again demonstrate their competence during an inspection of the laboratory. ATCP 77.22(7)(e)(e) If a provisionally certified analyst fails a proficiency evaluation on a new set of proficiency samples, or is not present to demonstrate their competence during a biennial inspection of the laboratory, the department shall summarily suspend the analyst’s certification to perform that test. ATCP 77.22(8)(8) Restoring certification. The department may restore the certification of any analyst whose certification is summarily suspended under sub. (5) or (7) if the analyst completes a training program approved by the department and passes a proficiency evaluation under s. ATCP 77.24 on a new set of proficiency samples. The department shall restore the analyst to full certification, even if the analyst was conditionally certified when certification was suspended. ATCP 77.22(9)(9) List of certified analysts. The department shall maintain, for each certified laboratory, a list of analysts currently certified to perform tests listed under s. ATCP 77.02 (1) and (2). The list shall identify the tests which each analyst is certified to perform. ATCP 77.22(10)(a)(a) An operator shall notify the department within 30 days after any of the following occurs: ATCP 77.22(10)(a)1.1. An analyst certified under this section is no longer employed by the laboratory. ATCP 77.22(10)(a)2.2. There is a change in the name of any analyst certified under this section. ATCP 77.22(10)(b)(b) An operator shall notify the department of a staffing change within 7 days after that change occurs if, as a result of that change, the operator no longer meets applicable certification requirements under s. ATCP 77.08 (3). ATCP 77.22 HistoryHistory: Cr. Register, September, 1999, No. 525, eff. 10-1-99; r. (2) (b) and renum. (2) (c) to be (2) (b), Register, December, 1999, No. 528, eff. 1-1-00; emerg. r. and recr. (1), eff. 11-15-01; CR 01-124: r. and recr. (1) Register December 2002 No. 564, eff. 1-1-03; CR 19-076: r. and recr. (2), am. (3) (c), r. and recr. (7) Register May 2020 No. 773, eff. 6-1-20; renum. (intro.), (a), (b) to (am), 1., 2. under s. 13.92 (4) (b) 1., Stats., Register May 2020 No. 773 ATCP 77.23ATCP 77.23 Drug residues in milk; screening tests. ATCP 77.23(1)(a)(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). ATCP 77.23(1)(b)(b) The department may not approve a laboratory under par. (a) unless all of the following apply: ATCP 77.23(1)(b)1.1. The department has approved at least one individual under sub. (2) to perform the drug residue screening test at the approved laboratory. ATCP 77.23(1)(c)(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. ATCP 77.23(2)(a)(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). ATCP 77.23(2)(b)(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). ATCP 77.23(2)(c)(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). ATCP 77.23(3)(3) Approval fees. A laboratory operator shall pay the following fees to acquire and maintain a laboratory approval under sub. (1): ATCP 77.23(3)(b)(b) An initial fee of $180 if the laboratory tests milk for only one dairy plant operator and all the following apply: ATCP 77.23(3)(b)2.2. The dairy plant operator receives milk from not more than 5 producers. ATCP 77.23(3)(b)3.3. The dairy plant operator receives not more than 10,000 lbs. of raw milk per week. ATCP 77.23(3)(c)(c) An initial fee of $72 if the laboratory does not apply for approval to perform any visual read test. ATCP 77.23(3)(d)(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). ATCP 77.23(3)(e)(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). ATCP 77.23(3)(f)(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. ATCP 77.23(4)(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. ATCP 77.23 NoteNote: FDA 2400 series forms are on file with the department, the secretary of state and the legislative reference bureau.
ATCP 77.23(5)(a)(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. ATCP 77.23(5)(b)(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. ATCP 77.23(5)(c)(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: ATCP 77.23(5)(c)3.3. Deadlines for examining proficiency evaluation samples and reporting test results. ATCP 77.23(5)(d)(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. ATCP 77.23(5)(e)(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. ATCP 77.23(6)(6) Failed proficiency evaluation; loss of approval. ATCP 77.23(6)(a)(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. ATCP 77.23(6)(b)(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. ATCP 77.23(6)(c)(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. ATCP 77.23(7)(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. ATCP 77.23(8)(a)(a) A laboratory operator shall notify the department within 30 days after any of the following occurs: ATCP 77.23(8)(b)(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. ATCP 77.23 HistoryHistory: Emerg. cr. eff. 11-15-01; CR 01-124: cr. Register December 2002 No. 564, eff. 1-1-03; CR 07-006: r. and recr. (1), am. (3) (d) and (f), Register January 2008 No. 625, eff. 2-1-08; CR 07-037: am. (3) (a) and (c) to (e) Register April 2008 No. 628, eff. 5-1-08; CR 14-073: am. (1) (a), (b) 2. Register August 2016 No. 728, eff. 9-1-16; CR 19-076: am. (3) (a), (b) (intro.), (c) to (f) Register May 2020 No. 773, eff. 6-1-20. ATCP 77.24ATCP 77.24 Milk and food analysts; proficiency evaluation. ATCP 77.24(1)(1) Annual proficiency evaluation required. Except as provided in sub. (4), the department may not renew an analyst’s certification to perform any test listed under s. ATCP 77.02 (1) or (2) unless, within the year immediately preceding that renewal, the analyst passes a proficiency evaluation for that test. The proficiency evaluation shall comply with this section. ATCP 77.24(2)(2) Form of evaluation. In a proficiency evaluation under sub. (1), an analyst shall examine samples prepared by an approved evaluator under sub. (3). The contents of the samples shall be known only to the evaluator. The evaluator shall rate the analyst’s proficiency by comparing the analyst’s results to the known contents of the samples, and shall report those results and ratings to the department. The reported results and ratings are rebuttably presumed to be valid for purposes of s. ATCP 77.22 and this section. ATCP 77.24(3)(3) Approved evaluator. The department, or another evaluator approved by the department in writing, shall serve as a proficiency evaluator under sub. (2). ATCP 77.24 NoteNote: The department will approve an evaluator under sub. (3) if FDA approves that evaluator for the same purpose.
ATCP 77.24(4)(4) Evaluation procedure; general. A proficiency evaluation under sub. (1) shall be conducted according to a standard evaluation procedure which the department approves in writing. An analyst is not required to complete a proficiency evaluation for any test unless the department has approved a standard evaluation procedure for that test. A standard evaluation procedure shall comply with applicable requirements under sub. (5), and shall include standards for all of the following: ATCP 77.24(4)(a)(a) The evaluator’s preparation of proficiency evaluation samples. ATCP 77.24(4)(b)(b) The analyst’s examination of proficiency evaluation samples. ATCP 77.24(4)(c)(c) Deadlines for examining proficiency evaluation samples and reporting test results. ATCP 77.24(4)(d)(d) The evaluator’s review and rating of the analyst’s proficiency. ATCP 77.24(5)(a)(a) Proficiency evaluations for the following tests under s. ATCP 77.02 (1) shall test include at least the following number of samples: ATCP 77.24(5)(a)1.1. At least six but not more than 20 samples for standard plate count, petrifilm aerobic count, plate loop count, petrifilm rapid aerobic count, peel plate aerobic count, or phosphatase tests. ATCP 77.24(5)(a)2.2. At least eight but not more than 20 samples for direct microscopic somatic cell counts, electronic somatic cell counts, drug residue tests, or coliform tests. ATCP 77.24(5)(b)(b) To pass a proficiency evaluation under par. (a) which involves 6 to 10 samples, an analyst shall obtain no more than one unacceptable sample result. To pass a proficiency evaluation under par. (a) which involves 11 to 20 samples, an analyst shall obtain no more than 2 unacceptable sample results. ATCP 77.24(5)(c)(c) In a proficiency evaluation for any of the following tests, a sample result is unacceptable if it falls outside the statistical limits established in FDA’s “Evaluation of Milk Laboratories,” 2017 edition:
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Chs. ATCP 55-89; Food, Lodging, and Recreation Safety
administrativecode/ATCP 77.23(2)
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