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

Qualified Person (QP)

  • UK Batch Release
  • New Product Due Diligence
  • EU/UK GMP Audit
  • QP Declaration
  • Expert GMP Compliance Assessment
  • GMP Training
  • Self-Inspection