GroundRules
16 CFR 1702.16: Petitions requesting an exemption for a drug or a new drug.
Where this section sits in the code
- Title 16—Commercial Practices
- CHAPTER II—CONSUMER PRODUCT SAFETY COMMISSION
- SUBCHAPTER E—POISON PREVENTION PACKAGING ACT OF 1970 REGULATIONS
- PART 1702—PETITIONS FOR EXEMPTIONS FROM POISON PREVENTION PACKAGING ACT REQUIREMENTS; PETITION PROCEDURES AND REQUIREMENTS
(a) Where the petition requests an exemption for a drug, as defined in section 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.
(b) [Reserved]
Collected 2026-08-27T02:24:29Z. Source file · JSON