RAPS is closely monitoring developments in the Coronavirus (COVID-19) outbreak. See our public safety page for the latest updates.

The RAPS store will be under maintenance Saturday, 13 June between 6 AM and 12 PM EST. Store functionality may be unavailable at times during this window.
We apologize for any inconvenience caused during this time.

(SOLD OUT) RAPS European Workshop on MDR

RAC Credits
Tuesday, 08 October 2019 (8:00 AM) - Wednesday, 09 October 2019 (3:30 PM) Amsterdam, Berlin, Bern, Rome, Stockholm, Vienna
Damrak 1-5, 1012 LG
Amsterdam, Netherlands


Through 8 September 2019
Member: €850
Nonmember: €950
From 9 September 2019 through 4 October 2019
Member: €950
Nonmember: €1050

*Netherlands charges 21% VAT
The new MDR will be effective in May 2020. This two-day workshop brings together thought leading medical device regulatory faculty for a hands-on discussion featuring exercises to review progress, share concerns and help make sense of the new expectations. This event is not an entry-level workshop but is a unique opportunity to review the requirements, understand the practical solutions and calibrate on how much data is needed to achieve compliance. Hear from others and share experiences gained in working through transition issues and confirm confidence through discussions and practical exercises with experts, peers, and colleagues. This workshop will be particularly valuable to all regulatory professionals responsible for achieving MDR compliance for both legacy CE MDD and innovative new medical devices intended for the European Market.
Learn More