Medical Devices GMP GDP IS0 13485 Auditing MIA WDA QP RP & RPi Regulatory Pharmacovigilance R&D Innovation
Medical Devices GMP GDP IS0 13485 Auditing MIA WDA QP RP & RPi Regulatory Pharmacovigilance R&D Innovation

Responsible Person (RP) and RPi (Responsible Person for Import)

  • GDP Audit
  • Expert RP Services for warehouse, distribution and supply chain management.
  • Contract Recall and Mock Recall Services.
  • GDP Training
  • Self-Inspection
  • RPi Batch Release for EU QP Certified Products.