21 CFR Part 812 · Investigational Device Exemptions

§ 812.10 Waivers

Subpart A - General Provisions Official text on eCFR Amendment history

(a) Request. A sponsor may request FDA to waive any requirement of this part. A waiver request, with supporting documentation, may be submitted separately or as part of an application to the address in § 812.19 .

(b) FDA action. FDA may by letter grant a waiver of any requirement that FDA finds is not required by the act and is unnecessary to protect the rights, safety, or welfare of human subjects.

(c) Effect of request. Any requirement shall continue to apply unless and until FDA waives it.

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FDA guidance that cites § 812.10

Amendment history

Federal Register documents that created or amended this section.