{"id":1078,"date":"2024-02-05T15:51:44","date_gmt":"2024-02-05T13:51:44","guid":{"rendered":"https:\/\/drs.nu\/?page_id=1078"},"modified":"2024-02-20T11:02:30","modified_gmt":"2024-02-20T09:02:30","slug":"hans-van-dulmen","status":"publish","type":"page","link":"https:\/\/drs.nu\/en\/hans-van-dulmen\/","title":{"rendered":"Hans van Dulmen"},"content":{"rendered":"

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Hans van Dulmen<\/h1>\n

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Hans van Dulmen is founder and director of DRS. He graduated in Electrical Engineering and Business Administration and has held various positions in the past 20 years in the medical devices industry. He started out working in the development of high-risk medical products. Then he held management positions over 15 years in the field of regulatory and clinical testing in both cardiovascular and tissue engineering firms.<\/div>\n<\/div>\n<\/div>\n

[\/vc_column_text][\/vc_column][vc_column width=”1\/3″][vc_column_text]Hans has been a member of industry associations such as EUCOMED. He plays an active role in standard committees for clinical research (EN ISO 14155) and medical electrical equipment (IEC 601 series by Dutch Standard Commission of a TC62) and the Dutch Association of Research QA (DARQA). Hans specializes in clinical evidence, risk management, CE marking and FDA submissions.[\/vc_column_text][\/vc_column][vc_column width=”1\/3″][vc_column_text]Through work experience and a large number of specialist training Hans van Dulmen acquired a great deal of knowledge and developed a distinctive approach. His view is that DRS must not only ensure that the products can be placed on the market in accordance to the regulations, but also that companies are able to pragmatically give legislation a permanent place in their development process. Hans van Dulmen is your contact for all projects, even when these are (co-)carried out by project staff.[\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

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