This online course will show you how to write scientific documents such as a clinical evaluation in good and readable English that is appropriate to your audience, while complying with the regulatory requirements.
How to prepare effectively for the responsibilities of a person responsible for regulatory compliance (PRRC). This and more in our online-seminar via Zoom!
This seminar provides information on early access programmes, HTA requirements, CUP and off-label use in Europe
Would you like to successfully approve and market your medical devices in China as well? Then attend our webcats and learn more about market potential, product approvals and customs regulations. Our local expert will provide you with comprehensive information - especially on the subject of approval and risks that exist for European medical device manufacturers or importers.
This seminar addresses the regulatory and import essentials, and what needs to be done for successful entry into the Russian market.
Basic and advanced know-how on the current regulatory framework of the various countries will be addressed in this course.