21 CFR Part 58 - Good Laboratory Practice (GLP)
Records and Reports (Subpart J)

21 CFR Part 58 - Good Laboratory Practice (GLP) 58.185: Reporting of Nonclinical Laboratory Study Results

A final report must be prepared for each study with prescribed content including name and address of facility, dates, objectives, methods, deviations, statistical methods, results, and Study Director signature.

Other controls in Records and Reports (Subpart J)

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.

MCP endpointAll 21 CFR Part 58 - Good Laboratory Practice (GLP) controls