21 CFR Part 211 - Current Good Manufacturing Practice
Subpart J - Records and Reports

21 CFR Part 211 - Current Good Manufacturing Practice CFR211-J-198: Section 211.198 - Complaint Files

Written procedures describing the handling of all written and oral complaints regarding a drug product shall be established and followed. A written record of each complaint shall be maintained.

Other controls in Subpart J - Records and Reports

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