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.
This advanced seminar is designed as an advanced course and will focus on all relevant topics for an expert in the field of medical scientific information. Our speakers will update you on all the applicable key issues.
Our global and local experts will update you every two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs and pharmacovigilance at your fingertips!
This 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.
This international conference will take place on October 23 - 24, 2019. Stakeholders from every corner of the medical device world will meet in Amsterdam to discuss the latest trends and issues in regulatory affairs.