Do you need assistance for the (pre)market approval of your medical devices?
Your company wants to approach new markets?

PROSYSTEM AG will assist you to answer these and more questions and also help to find the easiest way for getting your medical devices market approval. We will help with all regulatory affairs questions in order to place your medical device into the correct category (also in the borderline sector), to place the product on the market in a timely manner and to maintain a valid state.
Together with our subsidiaries: PROSYSTEM USA LLC. and PROSYSTEM do Brasil Ltda. we are able to offer an extensive portfolio of on-site services to you. Benefit from our long years of experience in regulatory affairs and our knowledge on specific national approval processes, if you want to approach the Asian or Canadian market.

Please feel free to contact us for further details about regulatory affairs or a nonbinding quotation.

Also, do not miss the opportunity to attend one of our seminars, for example “#_CATNEXTEVENTSHORT”.