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IVDR Overview

Date & Time

from29-06-202109:00
until29-06-202112:00
duration3 hours

Location

placeOnline
cityLausanne, Schweiz

Contact

nameMr. Raimo SumpMedidee Services SA
phone0170 96 01 473
emailtraining@medidee.com

Training objectives:
The following skills and competencies are developed:

  • Overview of IVDR challenges compared to existing IVDD
  • Better understand the risk-benefit ratio approach
  • Identify applicable IVDR requirements and the impact on the quality management system
  • Identify applicable IVDR requirements and the impact on the technical file
  • Planning of Verification & Validation under IVDR

Training content:

  • IVDR structure and definitions
  • Key changes under IVDR and risk-benefit ratio approach
  • Transition timelines
  • New Classification rules
  • Structure of the Technical Documentation
  • General Safety and Performance Requirements (GSPR), what’s new?
  • Additional requirements on:
  1. Clinical Evidence and Performance Evaluation Report
  2. Post Market Surveillance
  3. Conformity Assessment