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Info on Electronic Labeling for Drugs, Biologics Sent to OMB

09/13/2013

Federal Register Notice: FDA’s proposed collection of information, “Requirements for Submission of Labeling for Human Prescription Drugs and Biologics in Electronic Format,” 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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