The essentials in Medical Writing the Clinical Study Report (CSR)
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!
e-Learning course with six modules on how to initiate and manage collaborations with patients and patient organisations successfully.
During this winter 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.
