21 CFR Part 11: Electronic Records; Electronic Signatures

FDA · In force

Last verified: not yet

Summary

The US regulation setting the conditions under which FDA treats electronic records and signatures as equivalent to paper records and handwritten signatures: validation, audit trails, access controls, record protection and signature controls.

Dated events

  1. 20 Aug 1997 Effective Source for Effective

Official source

Official text

Source: FDA. Public domain.