The market for medical devices is subject with respect to the initial authorization to place on the market and the production and marketing process, a variety of regulatory requirements. This also regular adjustments of documents and systems have to be associated. Additionally show currently at the legislative level in the current revision process for medical devices law other important changes.
This 2-day seminar on the current medical device law will give the beginner as well as to deepen your knowledge - both theoretical and practical - a comprehensive overview of national and European requirements, procedures, the implementation in the company and corresponding responsibilities and obligations for manufacturers and competent authorities. addressed here are in addition to the original medical device manufacturers also the pharmaceutical industry, which has put in the development and marketing of medical devices, material or combination of products in addition to the Medicines Act to deal with the medical device law. The demarcation of the product categories to each other is profound knowledge ahead in both jurisdictions.