No matter the continent or country, medical-device industry is always a challenge. Participants need to be familiar with the general legal framework as well as specific regulations. Above all, they must be able to fulfil their respective requirements. Our consultants have gathered significant knowledge and experience in the regulatory aspects of medical devices. Apart from individual consultancy, we also offer seminars and workshops to present general frameworks and procedures.
Below you can find our current workshops. Nevertheless, feel free to approach us with your specific seminar requests on any of our services.
|EUMMAN Seminar (english) | UK, France and Scandinvia||February 28th 2019||BVMed, Berlin|
|MDR Seminar (german)| Presenter: Karsten Nieter-Kubin (Head of Regulatory Affairs) and others||August 30th 2018||BEO MedConsulting, Berlin|
|HMV Seminar (german)| Presenter: Olaf Meyer (Head of Marketing and Sales)||tba||BVMed,|