Title 21 -- FOOD AND DRUGS
Chapter I -- FOOD AND DRUG ADMINISTRATION
Part 11 ELECTRONIC RECORDS; ELECTRONIC SIGNATURES
21 CFR Part 11 is a section in the Code of Federal Regulations (CFR) that outlines the US Food and Drug Administration’s (FDA) guidelines on using electronic records and electronic signatures. Here’s the exhaustive guide from the FDA, if you’re into long documents. Each title of the CFR addresses a different regulated area, 21 CFR relates to Pharmaceuticals and Medical Devices and Part 11 addresses electronic records and electronic signatures.
At the most general level, Part 11 is a law that ensures that companies and organizations implement good business practices by defining the criteria under which electronic records and signatures are considered to be accurate, authentic, and equivalent to paper records and handwritten signatures on paper. Part 11 essentially allows an electronic record to take the place of a paper record, and allows any handwritten signature to be replaced by an electronic signature.
What the definitions are…
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