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

What does CFR211-I-166 require?

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.

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

Other controls in Subpart I - Laboratory Controls

Query this from an agent

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