RAPS 2020 European Workshops

RAPS European Workshops

Developed by European regulatory professionals for regulatory professionals operating in Europe’s quickly changing and uncertain regulatory environment, RAPS European workshops bring together leading experts in the medical device, IVD and pharmaceutical industries.

Join us for one of the workshops below to gain insight into some of the most urgent and crucial issues facing regulators, manufacturers and regulatory professionals working with healthcare products for the European market.

 
Post-Market Surveillance in Europe

Post-Market Surveillance in Europe

9 March 2021
9:00–16:00 CET

 6.0   RAC CREDITS

With the imminent approach of EU MDR's implementation deadline, companies that sell Medtech products within the EU need to prepare for drastic change. Meeting the new regulations' demands, especially for post-market surveillance, will consume more time and resources than ever before. Companies should investigate the available tools and technologies for achieving post-market surveillance compliance effectively and efficiently in preparation. Gain an in-depth understanding and learn actionable tips and strategies for saving time and money while achieving post-market surveillance compliance under the new EU MDR.

 
Design Controls and Human Factors

Design Controls and Human Factors

17–19 March 2021
15:00–19:00 CET

 12.0   RAC CREDITS

This interactive workshop is designed to take participants through the design control elements, emphasizing how human factors fits into each step in the design process.

 
Data Management and Digitalization in Regulatory Affairs

Data Management and Digitalization in Regulatory Affairs

24 March 2021
9:00–17:00 CET

 8.0   RAC CREDITS

The workshop is an open debate allowing the regulators and industry to find common approaches for addressing the increasing complexity of the medical devices industry.