Overview of Medical Device Regulation in Europe 2018 is a webinar dedicated to to review critical elements of the new regulations and is suitable for clinical, regulatory and quality leaders.
Overview of Medical Device Regulation in Europe 2018 covers topics such as:
- Regulations and their impact on CERs (Clinical Evaluation Reports)
- Medical Device Regulation in Europe – background
- How to design Clinical Trials, including how the MDR will affect post market clinical studies for existing products
Overview of Medical Device Regulation in Europe 2018 intended for:
- Regulatory affairs
- Quality managers
- Clinical managers
- Manufacturers
- Project managers
- Product development managers