---
kind: "section"
citation: "21 C.F.R. § 1.1410"
title: "21"
number: "1.1410"
heading: "When will FDA consider whether to waive a requirement of this subpart?"
url: "https://uscodex.org/cfr/21/1.1410"
---

# §1.1410. When will FDA consider whether to waive a requirement of this subpart?


FDA will consider whether to waive a requirement of this subpart on our own initiative or in response to the following:

- (a) A written request for a waiver for an individual entity; or
- (b) A citizen petition requesting a waiver for a type of entity submitted under [§ 10.30](/cfr/21/10.30.md) of this chapter by any person subject to the requirements of this subpart.

## Notes

### 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.