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

MIA

  • Contract QP Batch Release
  • Importation and market release of pharmaceutical product from Non-EU and EU Countries.
  • Provide QC testing services through approved (MIA) UK/EU QC testing Lab.