21 CFR Part 211 - Current Good Manufacturing Practice
Subpart I - Laboratory Controls

21 CFR Part 211 - Current Good Manufacturing Practice CFR211-I-170: Section 211.170 - Reserve Samples

What does CFR211-I-170 require?

An appropriately identified reserve sample shall be retained for each lot of each drug product. The reserve sample shall be stored under conditions consistent with product labeling.

Maintained by Gerard BlokdykVerified against the published standard Control text last updated

Other controls in Subpart I - Laboratory Controls

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