Audit Docs conducts GMP/GLP/GDP/GCP/GAP Assessment audits for FDF, API, Intermediate, KSM, Packaging material, Nutraceutical manufacturing facilities and Clinical research organisations in accordance with ICH Q7, PIC/S, ISO, 21 CFR Part 11, 210, 211 and EudraLex Vol 4 guidelines. Audit Docs have over 25 experienced and APIC, ECA, ASQ, CQI-IRCA certified auditors to perform the audits as per the customer requirement. All our audit reports are well accepted by QPs and regulatory authorities across the globe.

Our quality auditing process starts with collecting required information from the client and facility, preparing an agenda and checklist, executing the audit, and providing a complete audit report package that includes an executive summary report with audit observations, a detailed audit report, CAPA review reports and an audit closure statement.