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Info on Medicated Articles CGMPs Sent to OMB

06/20/2014

Federal Register Notice: FDA’s proposed collection of information, “Current Good Manufacturing Practice Regulations for Type A Medicated Articles — 21 CFR Part 226,” 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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