When: 10 – 11 June | 09:00 - 17:00 Eastern Daylight Time (US/Canada) (GMT -4)
Where: Online
Event overview
TOPRA and The Regulatory Affairs Professionals Society (RAPS) are partnering for their second joint workshop, RAPS/TOPRA Inter-regulatory and Stakeholder Workshop: Alignment of Global ‘Combination’ Products Regulations.
By bringing together regulatory affairs professional leaders, the workshop will provide a consistent global approach regarding the most pressing topics you need to know about the new Medical Device Directive (MDR) and 'combination' products. Our diverse panel of speakers includes representatives of the European Commission, Member State medicinal and medical device authorities, Notified Bodies, FDA officials, and industry experts to explore the complex issue of MDR.
This workshop will include a full review of the changes the MDR will bring and explore the impact the MDR will have on:
- Legislative background and state-of-play guidance and interpretation
- Device primary mode of action
- Drug primary mode of action
There will be ample opportunities for stakeholder discussion and conclusions. Don't miss your chance to have your say during this important workshop!
Programme and speakers
Visit the RAPS website for a more detailed breakdown of the agenda and participants for this event.
Pricing
- RAPS / TOPRA Members: $714 *
- Non-members: $824
* To receive your TOPRA member discount when registering for the course, please use the discount code COMBO20 during checkout.
How to register
Registration for this event is available on the RAPS website.
Register now