3rd Regulatory workshop

 

When: 16th November 2017

Where: Berlin in the frame of Frontiers Health

Format: The Regulatory Awareness Workshop (RAW) focuses on the medical device regulatory landscape that arises to startups and SMEs in the digital health sector. The RAW helps developers of medical and health-related apps and software to understand the importance of considering the medical device regulatory framework in the digital health sector.

By using case studies, the following issues are explained:

– when medical software falls under the medical device directive

– how to classify medical device software

– which key regulatory standards are mandatory

– the impact of the new regulation (MDR) on medical device software

The presentation is followed by a Q&A section.

 

The registrations for this eHealth Hub event will open soon!

Get ready!

 

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