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Info on Supplement CGMPs Sent to OMB

12/02/2014

Federal Register Notice: FDA’s proposed collection of information “Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements — 21 CFR 111.75(a)(1)(ii),” has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. To view this notice, click here.

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