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Info on GLPs for Nonclinical Studies Sent to OMB

07/14/2011

Federal Register Notice: FDA’s proposed collection of information, “Good Laboratory Practice Regulations for Nonclinical Studies — 21 CFR Part 58,” 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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