Seminare zu Legal affairs & marketing
Legal affairs & marketing
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Scientific Writing for Medical Devices

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.

  • online / 13. - 14.05.2020

The Person Responsible for Regulatory Compliance

How to prepare effectively for the responsibilities of a person responsible for regulatory compliance (PRRC). This and more in our online-seminar via Zoom!

  • online / 14.05.2020

Patient Access: Early Access, Compassionate Use, Off-label Use

This seminar provides information on early access programmes, HTA requirements, CUP and off-label use in Europe

  • Frankfurt / 30.06.2020

Medical Devices in China

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.

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Market Access of drugs in Russia

This seminar addresses the regulatory and import essentials, and what needs to be done for successful entry into the Russian market.

  • Berlin / 28.09.2020

Marketing Authorisation in ASIA

Basic and advanced know-how on the current regulatory framework of the various countries will be addressed in this course.

  • Mannheim / 20. - 22.10.2020
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