This hour long Webinar will cover an overview of the changes to the European Medical Device regulations. It will explore the key drivers of the regulation change, and what that means for organizations going forward. The webinar will also cover the importance of educating teams now to be ready for the 2020 deadline.
3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS (Recorded)
- Training
- 3 Hours
- Europe, United States Europe, United States
