krankenhaus-it.de created an overview of KHZG players in the German market. Find the list of players for each „Fördertatbestand“ here
Here you can find a list of notified bodies in Europe: For the list click here
There are numerous QM (Quality Management) and RA (Regulatory Affairs) consultancies that assist medical device companies with the implementation of ISO standards such as ISO 13485, reimbursement issues, technical documentation, PSM (Post Market Surveillance) and much more:
There are numerous companies that specialise in developing medical devices. For start-ups in particular, such partners are experienced experts who know how to develop a medical device. Nevertheless, a lot of knowledge is required in the start-up itself; it is not possible to simply outsource the development, you have to know yourself what exactly you …
