Food and Drug Administration, HHS.
The Food and Drug Administration (FDA) is announcing that a collection of information entitled “Guidance for Industry on User Fee Waivers, Reductions, and Refunds for Drug and Biological Products” has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
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FOR FURTHER INFORMATION CONTACT:
FDA PRA Staff, Office of Operations, Food and Drug Administration, 8455 Colesville Rd., COLE-14526, Silver Spring, MD 20993-0002, PRAStaff@fda.hhs.gov.
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On July 16, 2014, the Agency submitted a proposed collection of information entitled “Guidance for Industry on User Fee Waivers, Reductions, and Refunds for Drug and Biological Products” to OMB for review and clearance under 44 U.S.C. 3507. An Agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910-0693. The approval expires on August 31, 2017. A copy of the supporting statement for this information collection is available on the Internet at http://www.reginfo.gov/public/do/PRAMain.
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Dated: October 1, 2014.
Assistant Commissioner for Policy.
[FR Doc. 2014-23842 Filed 10-6-14; 8:45 am]
BILLING CODE 4164-01-P