The date of application of the new EU Medical Device Regulation (MDR) is nearing. Preparing for smoothly transitioning to the MDR is vital for assuring business continuity and sales in the EU. This webinar will provide participants with a comprehensive overview of the new requirements and a practical step by step guide to prepare for the transition. Lessons learned from on-going transition programs of major medical device manufacturers will be shared with the audience.
- Overview of the major changes brought forward by the new MDR
- Schedule, timelines and validity of certificates issued
- Step by step guide for successful transition
- Tips dispensed based on our experience in prepping manufacturers for the transition
- Medical Device Manufacturers
- Management Teams
- Quality Departments
- Regulatory Affairs Departments
- Manufacturing Departments
- Engineering Departments
- Marketing and Sales Departments
- Clinical Professionals
MD3094