API audits to assess GMP compliance

Diapharm ensures that suppliers of APIs, starting materials and excipients will be audited in a cost-efficient manner. We offer accredited third-party API audits worldwide via Europe’s first accredited inspection body for active pharmaceutical ingredients.

Our services

  • Coordination of independent, high-quality shared third-party API audits by qualified auditors – see our audit schedule
  • Comprehensive audit reports
  • Management of deviations (CAPA assessment and response)
  • Confidentiality on all levels and guaranteed absence of conflict of interest
  • All costs (travel expenses) included in the price

Your benefits

  • Time and money saved on audits
  • Independent, accredited verification of GMP compliance
  • Decreased workload for the qualified person
  • Internationally recognised API audit reports
  • Reduced number of audits for manufacturers and clients

Highest quality

Our accredited third-party API audits meet the highest standards and are performed by an independent ISO 17020 (type A) accredited inspection body to ensure the highest quality and acceptance by the authorities.

Contact us for further information for audit schedules at auditsNOSPAM@diapharm.com! Or send us a message with the contact form under: Get in touch with us!