[Federal Register Volume 78, Number 230 (Friday, November 29, 2013)] [Notices] [Pages 71623-71624] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 2013-28598] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2013-N-0716] Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Designated New Animal Drugs for Minor Use and Minor Species 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: Fax written comments on the collection of information by December 30, 2013. ADDRESSES: To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer, FAX: 202-395-7285, or emailed to [email protected]. All comments should be identified with the OMB control number 0910-0605. Also include the FDA docket number found in brackets in the heading of this document. FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations, Food and Drug Administration, 1350 Piccard Dr., PI50-400B, Rockville, MD 20850, [email protected]. 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. Designated New Animal Drugs for Minor Use and Minor Species; 21 CFR Part 516--(OMB Control Number 0910-0605)--Extension Description: The Minor Use and Minor Species Animal Health Act of 2004 (MUMS) (Pub. L. 108-282) amended the Federal Food, Drug, and Cosmetic Act (the FD&C Act) to authorize FDA to establish new regulatory procedures intended to make more medications legally available to veterinarians and animal owners for the treatment of minor animal species as well as uncommon diseases in major animal species. This legislation provides incentives designed to help pharmaceutical companies overcome the financial burdens they face in providing limited-demand animal drugs. These incentives are only available to sponsors whose drugs are ``MUMS-designated'' by FDA. Minor use drugs are drugs for use in major species (cattle, horses, swine, chickens, turkeys, dogs, and cats) that are needed for diseases that occur in only a small number of animals either because they occur infrequently or in limited geographic areas. Minor species are all animals other than the major species; for example, zoo animals, ornamental fish, parrots, ferrets, and guinea pigs. Some animals of agricultural importance are also minor species. These include animals such as sheep, goats, catfish, and honeybees. Participation in the MUMS program is completely optional for drug sponsors so the associated paperwork only applies to those sponsors who request and are subsequently granted ``MUMS designation.'' The rule specifies the criteria and procedures for requesting MUMS designation as well as the annual reporting requirements for MUMS designees. Section 516.20 (21 CFR 516.20) provides requirements on the content and format of a request for MUMS-drug designation; Sec. 516.26 (21 CFR 516.26) provides requirements for amending MUMS-drug designation; provisions for change in sponsorship of MUMS-drug designation can be found under Sec. 516.27 (21 CFR 516.27); under Sec. 516.29 (21 CFR 516.29) are provisions for termination of MUMS-drug designation; under Sec. 516.30 (21 CFR 516.30) are requirements for annual reports from sponsor(s) of MUMS-designated drugs; and under Sec. 516.36 (21 CFR 516.36) are provisions for insufficient quantities of MUMS-designated drugs. Description of Respondents: Pharmaceutical companies that sponsor new animal drugs. In the Federal Register of July 2, 2013 (78 FR 39734), FDA published a 60-day notice requesting public comment on the proposed collection of information. No comments were received. FDA estimates the burden of this collection of information as follows: Table 1--Estimated Annual Reporting Burden \1\ ---------------------------------------------------------------------------------------------------------------- Number of 21 CFR Section Number of responses per Total annual Average burden Total hours respondents respondent responses per response ---------------------------------------------------------------------------------------------------------------- 516.20; Content and format of 15 5 75 16 1,200 MUMS request................... 516.26; Requirements for 3 1 3 2 6 amending MUMS designation...... 516.27; Change in sponsorship... 1 1 1 1 1 [[Page 71624]] 516.29; Termination of MUMS 2 1 2 1 2 designation.................... 516.30; Requirements for annual 15 5 75 2 150 reports........................ 516.36; Insufficient quantities. 1 1 1 3 3 ------------------------------------------------------------------------------- Total....................... .............. .............. .............. .............. 1,362 ---------------------------------------------------------------------------------------------------------------- \1\ There are no capital costs or operating and maintenance costs associated with this collection of information. The burden estimate for this reporting requirement was derived in our Office of Minor Use and Minor Species Animal Drug Development by extrapolating the current investigational new animal drug/new animal drug application reporting requirements for similar actions by this same segment of the regulated industry and from previous interactions with the minor use/minor species community. Dated: November 22, 2013. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2013-28598 Filed 11-27-13; 8:45 am] BILLING CODE 4160-01-P