16 CFR 1702.16 - Petitions requesting an exemption for a drug or a new drug.
(a) Where the petition requests an exemption for a drug, as defined insection 201(g)(1) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321(g)(1), the petitioner shall include those reports required to be filed under the Food and Drug Administration's Adverse Reaction Reporting Program.
[45 FR 13064, Feb. 28, 1980, as amended at 66 FR 40115, Aug. 2, 2001]
Title 16 published on 2015-01-01.
No entries appear in the Federal Register after this date, for 16 CFR Part 1702.