Combination Products Registration 2017 is a webinar that covers topics such as:
- CE Marking
- EU/US
- Documentation requirements for combination products EU/US
- 510 K and PMAs general Overview
- Managing third parties and document control
- Interfacing,Development,Quality,Regulatory
- Vigilance and adverse event reporting
Combination Products Registration 2017 is intended for:
- Medical Officers
- Regulatory Affairs