The GMED video series to prepare your transition to the medical device regulations.
This solution enables manufacturers and authorized representatives to best prepare their strategy by aligning the submission of their MDR certification projects with the requirements of the new regulations and the GMED certification process.
→ MODULE 1: PRE-APPLICATION PHASE
→ MODULE 2: FORMAL APPLICATION PHASE FOR CERTIFICATION
→ MODULE 3: CONFORMITY ASSESSMENT PHASE
→ MODULE 4: DECISION PHASE
→ MODULE 5: POST-CERTIFICATION MONITORING AND CONTROL PHASE