An up-to-date overview of and insights into supplier management for medical devices and related activities: Find the right balance between compliance, costs and quality, and learn how to implement your own effective vendor management.
Online Seminar series about Pharmaceutical Law in the EU
Medical Devices: Marketing authorisation and market access in Saudi Arabia, the UAEand Jordan. Don't miss out on this unique course! First-hand information provided by experienced speakers to guarantee market success of your enterprise.
The online course will show you how to write scientific and clinical documents such as a technical documentation or clinical evaluation in good and readable English that is appropriate to your audience, while complying with the regulatory requirements.
Would you like to successfully resist on Chinese market for medical devices? Then attend our webcasts and learn more about the new Chinese regulation for medical devices, how to perfect your pre-market registration and post-market surveillance: Our local experts will provide you with brandnew information!
Evidence generation, value proposition and the HTA - the latest insights with regard to Orphan Drugs
Online Seminar about Generic Market Access & Pricing in Europe
Compassionate Use Programme (CUP) and Named Patient Programme (NPP) - the expertise required to plan and conduct expanded access programmes.
How to prepare effectively for the responsibilities of a person responsible for regulatory compliance (PRRC). This and more in our online-seminar via Zoom!
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