Webinar about new European Regulations

Get the latest updates on the new Rgulations Webinar, 12 June, 5.00 - 6.00 p.m. (GMT +2)

Although it is not yet precisely clear what will be decided in Brussels, the medical device industry is undoubtedly facing several changes to Medical Device Regulations. DEKRA is pleased to invite you to join an exclusive client webinar in which we will inform you about the latest routing and approval process of the new Regulations, as well as the possible consequences for your organisation. Furthermore, you will receive an update on the progress of the “immediate measures” formulated by former European Commissioner Mr. Dalli as a consequence of the PIP scandal. 

Our key industry experts will translate the latest developments into valuable insights into the new Regulations and what they mean for you.

Needless to say, our experts will also be at your disposal to answer questions during the webinar. If you have any specific questions in regard to the new European Regulations, please already submit them when registering. 

Keen to learn how a webinar works? Click here!

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manufacturers all over the world in meeting complex regulatory requirements. We are proud to be one of the five largest Notified Bodies in the world. The quality level, expertise and service of DEKRA are a benchmark in the medical device certification industry. DEKRA guides you through the certification process.

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