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

21 CFR Part 211 - Current Good Manufacturing Practice CFR211-I-166: Section 211.166 - Stability Testing

There shall be a written testing program designed to assess the stability characteristics of drug products. Results shall be used to determine appropriate storage conditions and expiration dates.

Other controls in Subpart I - Laboratory Controls

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The graph holds this control, the 0 it maps to, and the evidence behind each claim, over MCP and REST.