StacksVerified U.S. regulatory reference

21 CFR §1.1410

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov
FDA will consider whether to waive a requirement of this subpart on our own initiative or in response to the following:
  1. (a)A written request for a waiver for an individual entity; or
  2. (b)A citizen petition requesting a waiver for a type of entity submitted under § 10.30 of this chapter by any person subject to the requirements of this subpart.