The definitions set forth in § 210.3 of this chapter apply in this part.
21 CFR Part 211 · Current Good Manufacturing Practice for Finished Pharmaceuticals
§ 211.3 Definitions
Independent copy, not an official legal edition. 21 CFR is a U.S. Government work in the public domain; this text comes from the eCFR and the annual CFR edition, and may lag recent amendments. The authoritative version is on ecfr.gov. Compliome is not affiliated with or endorsed by FDA. Not legal advice.
FDA guidance that cites § 211.3
Amendment history
Federal Register documents that created or amended this section.
- 43 FR 45077 29 Sept 1978