21 CFR Part 58 - Good Laboratory Practice (GLP)
Test Articles and Protocol (Subparts F & G)

21 CFR Part 58 - Good Laboratory Practice (GLP) 58.130: Conduct of a Nonclinical Laboratory Study

The study must be conducted in accordance with the protocol. All data must be recorded directly, promptly, and legibly in ink. Each data entry must be dated and signed or initialed.

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

What else in your programme already covers this

This control maps to 1 controls across 1 other frameworks. If you already hold one of them, the evidence you collected for it is the starting point here rather than new work.

  • 211.100 Written Procedures for Production and Process Control

Every mapping shown was judged rather than inferred from wording similarity, and the ones that failed review are published too. See the coverage reports and what was rejected.

Other controls in Test Articles and Protocol (Subparts F & G)

Query this from an agent

The graph holds this control, the 1 it maps to, and the evidence behind each claim, over MCP and REST.