Welcome to Medspero Group of Companies

Auditing & QA

Medical Device Management

  • To follow clear regulatory pathway for approval of Medical Device
  • To perform In-Vitro Device Regulation as a Consultancy Services
  • Transition services from MDD to MDR, maintaining compliance to
  • MDR 2017/745
  • Transition services from IVDD to IVDR
  • Gap Analysis for new regulation
  • New MDR and IVDR consultation services
  • Technical Documentation
  • Labelling reviews and updates
  • Unique Device Identification or UDI creation service