manufacturing-compliance

Audit manufacturing software for FDA 21 CFR Part 11 (electronic records, e-signatures, audit trails), ISO 9001/13485/14001/45001 quality management (document control, CAPA, nonconformance), GMP batch records and cleaning validation, lot/serial traceability (forward, backward, process, recall-ready), OSHA safety (incident tracking, LOTO, PPE), hazmat handlin…

Independent GitHub snapshot · Automated classification · Original documentation governs