The course is addressed to people new to regulatory affairs who want to acquire a comprehensive foundation; to regulatory professionals wishing to update their knowledge, and to all collaborators working in close relationship with regulatory affairs and wishing to understand the role of the department.

The patient has a unique expertise: “being a patient.” But how can they put this expertise to good use, for their peers as well as in contributing to integrated participation in research, education and advice? 

The how, the why and the who: all you would like to know about the MSL (Medical Science Liaison). This webinar is aimed at life science professionals who are not very familiar with this role or who would like to learn more on it.

We are very excited to welcome you this fall to our CLINICAL CONFERENCE - formerly known as the ACRP EUROPEAN CONFERENCE - on October 20, 2022 at the Park Inn by Radisson Brussels Airport. Closed for registration.

This session is the second part of a two-part training course on the “Sources of life sciences regulation”. It serves to provide participants with a high-level overview of the rules and regulations applicable to medicinal products for human use in the European Union. The session will include a specific part on the Belgian legislation. It will also provide the audience with practical tips on researching applicable laws.

During this webinar, we will focus on how to use the Investigator's Brochure to de-risk a First-in-Human (FIH) trial.  Speakers: Prof. Dr. Jan de Hoon and Dr. Thomas Lodeweyckx (UZ Leuven)