Pharmaceutical Auditing Services

Auditing services for the pharmaceutical industry: Our pharmaceutical audits are conducted in accordance with the relevant regulatory texts or standards, including GMP, GDP, GLP, GCP, and GVP. We also audit against IPEC guidelines for Pharmaceutical excipients, ISO 22716 (Cosmetics — Good Manufacturing Practices), EFfCI GMP for cosmetic ingredients, ISO 15378 standard for packaging materials, ISO 13485 standard for Medical devices, ISO 9001 standard or EHPM Quality guide for food supplements. 
Intertek's flexible solutions include private or individual audits, shared audits, CAPA evaluation and follow-up, audit report purchase, remote audits and support for your internal audit program. We audit suppliers and manufacturers of APIs, excipients, packaging materials and other materials, subcontractors of manufacturing, packaging, analytical testing, service providers of clinical trials (CROs), pharmacovigilance, transporters, IT service, cleaning service and all other services.

To learn more, visit our website:

www.intertek.com/pharmaceutical/auditing