Rules and Regulations. Notice
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/register/2023/07/21/2023-15487A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
BILLING CODE 4164-01-P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2010-N-0601] Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Current Good Manufacturing Practice Regulations for Medicated Feeds AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration
(FDA)is announcing that a proposed collection of information has been submitted to the Office of Management and Budget
(OMB)for review and clearance under the Paperwork Reduction Act of 1995. DATES: Submit written comments (including recommendations) on the collection of information by August 21, 2023. ADDRESSES: To ensure that comments on the information collection are received, OMB recommends that written comments be submitted to *https://www.reginfo.gov/public/do/PRAMain.* Find this particular information collection by selecting “Currently under Review—Open for Public Comments” or by using the search function. The OMB control number for this information collection is 0910-0152. Also include the FDA docket number found in brackets in the heading of this document. FOR FURTHER INFORMATION CONTACT: Amber Sanford, Office of Operations, Food and Drug Administration, Three White Flint North, 10A-12M, 11601 Landsdown St., North Bethesda, MD 20852, 301-796-8867, *PRAStaff@fda.hhs.gov.* SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed collection of information to OMB for review and clearance. Current Good Manufacturing Practice Regulations for Medicated Feeds—21 CFR Part 225 OMB Control Number 0910-0152—Extension Under section 501 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 351), FDA has the statutory authority to issue current good manufacturing practice
(CGMP)regulations for drugs, including medicated feeds. Medicated feeds are administered to animals for the prevention, cure, mitigation, or treatment of disease, or growth promotion and feed efficiency. Statutory requirements for CGMPs have been codified under part 225 (21 CFR part 225). Medicated feeds that are not manufactured in accordance with these regulations are considered adulterated under section 501(a)(2)(B) of the FD&C Act. Under part 225, a manufacturer is required to establish, maintain, and retain records for a medicated feed, including records to document procedures required during the manufacturing process to assure that proper quality control is maintained. Such records would, for example, contain information concerning receipt and inventory of drug components, batch production, laboratory assay results ( *i.e.,* batch and stability testing), labels, and product distribution. This information is needed so that FDA can monitor drug usage and possible misformulation of medicated feeds to investigate violative drug residues in products from treated animals and to investigate product defects when a drug is recalled. In addition, FDA will use the CGMP criteria in part 225 to determine whether the systems and procedures used by manufacturers of medicated feeds are adequate to ensure that their feeds meet the requirements of the FD&C Act as to safety, and also that they meet their claimed identity, strength, quality, and purity, as required by section 501(a)(2)(B) of the FD&C Act. A license is required when the manufacturer of a medicated feed involves the use of a drug or drugs that FDA has determined requires more control because of the need for a withdrawal period before slaughter or because of carcinogenic concerns. Conversely, a license is not required, and the recordkeeping requirements are less demanding, for those medicated feeds for which FDA has determined that the drugs used in their manufacture need less control. Respondents to this collection of information are commercial feed mills and mixers/feeders. In the **Federal Register** of February 6, 2023 (88 FR 7741), FDA published a 60-day notice requesting public comment on the proposed collection of information. Although one comment was received, it was not responsive to the four collection of information topics solicited. FDA estimates the burden of this collection of information as follows: Table 1—Estimated Annual Recordkeeping Burden [Registered licensed commercial feed mills] 1 21 CFR section; activity Number of respondents Number of responses per respondent Total annual responses Average burden per response Total hours 225.42(b)(5) through
(8)requires records of receipt, storage, and inventory control of medicated feeds 791 260 205,660 1 205,660 225.58(c) and
(d)requires records of the results of periodic assays for medicated feeds that are in accord with label specifications and also those medicated feeds not within documented permissible assay limits 791 45 35,595 0.5 (30 minutes) 17,798 225.80(b)(2) requires that verified medicated feed label(s) be kept for 1 year 791 1,600 1,265,600 0.12 (7 minutes) 151,872 225.102(b)(1) through (5), requires records of master record files and production records for medicated feeds 791 7,800 6,169,800 0.08 (5 minutes) 493,584 225.110(b)(1) and
(2)requires maintenance of distribution records for medicated feeds 791 7,800 6,169,800 0.02 (1 minute) 123,396 225.115(b)(1) and
(2)requires maintenance of complaint files by the medicated feed manufacturer 791 5 3,955 0.12 (7 minutes) 475 Total 992,785 1 There are no capital costs or operating and maintenance costs associated with this collection of information. Table 2—Estimated Annual Recordkeeping Burden [Registered licensed mixer/feeders] 1 21 CFR section; activity Number of recordkeepers Number of records per recordkeeper Total annual records Average burden per recordkeeping Total hours 225.42(b)(5) through
(8)requires records of receipt, storage, and inventory control of medicated feeds 100 260 26,000 0.15 (9 minutes) 3,900 225.58(c) and
(d)requires records of the results of periodic assays for medicated feeds that are in accord with label specifications and also those medicated feeds not within documented permissible assay limits 100 36 3,600 0.5 (30 minutes) 1,800 225.80(b)(2) requires that verified medicated feed label(s) be kept for 1 year 100 48 4,800 0.12 (7 minutes) 576 225.102(b)(1) through
(5)requires records of master record files and production records for medicated feeds 100 260 26,000 0.4 (24 minutes) 10,400 Total 16,676 1 There are no capital costs or operating and maintenance costs associated with this collection of information. Table 3—Estimated Annual Recordkeeping Burden [Nonregistered non-licensed commercial feed mills] 1 21 CFR section; activity Number of recordkeepers Number of records per recordkeeper Total annual records Average burden per recordkeeping Total hours 225.142 requires procedures for identification, storage, and inventory control (receipt and use) of Type A medicated articles and Type B medicated feeds 4,357 4 17,428 1 17,428 225.158 requires records of investigation and corrective action when the results of laboratory assays of drug components indicate that the medicated feed is not in accord with the permissible assay limits 4,357 1 4,357 4 17,428 225.180 requires identification, storage, and inventory control of labeling in a manner that prevents label mix-ups and assures that correct labels are used for medicated feeds 4,357 96 418,272 0.12 (7 minutes) 50,193 225.202 requires records of formulation, production, and distribution of medicated feeds 4,357 260 1,132,820 0.65 (39 minutes) 736,333 Total 821,382 1 There are no capital costs or operating and maintenance costs associated with this collection of information. Table 4—Estimated Annual Recordkeeping Burden [Nonregistered non-licensed mixer/feeders] 1 21 CFR section; activity Number of recordkeepers Number of records per recordkeeper Total annual records Average burden per recordkeeper Total hours 225.142 requires procedures for identification, storage, and inventory control (receipt and use) of Type A medicated articles and Type B medicated feeds 3,400 4 13,600 1 13,600 225.158 requires records of investigation and corrective action when the results of laboratory assays of drug components indicate that the medicated feed is not in accord with the permissible assay limits 3,400 1 3,400 4 13,600 225.180 requires identification, storage, and inventory control of labeling in a manner that prevents label mix-ups and assures that correct labels are used for medicated feeds 3,400 32 108,800 0.12 (7 minutes) 13,056 225.202 requires records of formulation, production, and distribution of medicated feeds 3,400 260 884,000 0.33 (20 minutes) 291,720 Total 331,976 1 There are no capital costs or operating and maintenance costs associated with this collection of information. Our estimated burden for the information collection reflects an overall decrease of 10,435 hours and an increase of 831,545 records since the last OMB approval. We attribute this adjustment due to an increase in the number of non-registered, non-licensed commercial medicated feed mills and decrease in non-licensed medicated feed mill recordkeeping the last few years. Dated: July 17, 2023. Lauren K. Roth, Associate Commissioner for Policy. [FR Doc. 2023-15487 Filed 7-20-23; 8:45 am]
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- 21 CFR 225
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