PharmaFORUM Webcast Clinical Trials "Electronic data capture in NIS: Best practice"
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.
PharmaFORUM Webcast Clinical Trials "GCP for ATMP"
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!
During this Summer School you will build a solid toxicological know-how basis and will be informed about the inclusion of toxicological data in the marketing authorisation dossier. Take the chance and participate in our interactive online training.