§1.1410. When will FDA consider whether to waive a requirement of this subpart?
21 C.F.R. § 1.1410
FDA will consider whether to waive a requirement of this subpart on our own initiative or in response to the following:
A written request for a waiver for an individual entity; or
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.
Notes, amendments, and revision history
Source
Source: 87 FR 71077, Nov. 21, 2022, unless otherwise noted.
Authority
Authority: 15 U.S.C. 1333, 1453, 1454, 1455, 4402; 19 U.S.C. 1490, 1491; 21 U.S.C. 321, 331, 332, 333, 334, 335a, 342, 343, 350c, 350d, 350j, 352, 355, 360b, 360ccc, 360ccc-1, 360ccc-2, 362, 371, 374, 381, 382, 384a, 387, 387a, 387c, 393, and 2223; 42 U.S.C. 216, 241, 243, 262, 264, 271.
Source
Source: 42 FR 15553, Mar. 22, 1977, unless otherwise noted.