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Current as of January 02, 2025 | Updated by Findlaw Staff
When appropriate, time limits for the completion of each phase of production shall be established to assure the quality of the drug product. Deviation from established time limits may be acceptable if such deviation does not compromise the quality of the drug product. Such deviation shall be justified and documented.
Cite this article: FindLaw.com - Code of Federal Regulations Title 21. Food and Drugs § 21.211.111 Time limitations on production - last updated January 02, 2025 | https://codes.findlaw.com/cfr/title-21-food-and-drugs/cfr-sect-21-211-111/
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