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FDA Submits Info on Dietary Supplement AERs to OMB
01/21/2016
 

Federal Register Notice: FDA’s proposed collection of information, “Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act — 21 U.S.C. 379aa-1(b)(1),” 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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