21 CFR 211.111 - Time limitations on production.
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.
Title 21 published on 2014-04-01.
No entries appear in the Federal Register after this date, for 21 CFR Part 211.