Auditing of Producers of Medical Devices

Medical Devices Auditing

Medical Device producers face specific challenges to comply with stringent regulations and safety concerns when bringing their products to market.

On behalf of our clients who produce medical devices, Integrity Pharma Services performs audits and consulting services to ensure strict compliance to regulations and safety standards.

Our medical devices auditing program includes:

  • Medical Device Single Audit Program (MDSAP)
  • ISO 13485
  • Medical Device Directive (MDD)
  • Medical Device Regulation (MDR)
  • Cosmetics GMP – ISO 22716:2007

Contact Integrity Pharma Services for a consultation to learn how we can help you ensure compliance.