§ 1.1410. When will FDA consider whether to waive a requirement of this subpart?
62 words·~1 min read·
/us/cfr/t21/s§ 1.1410·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
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 of this chapter by any person subject to the requirements of this subpart.