During this Healixia workshop, different questions and ethical healthcare practices related to an offered hospitality (by pharma industry) to HCP’s for their participation to scientific events where they have the opportunity to keep abreast of trends in their profession, will be handled. Participants will be able to discuss cases in small groups and have a direct dialogue with Mdeon representatives.

This two-day course is intended to provide an in-depth knowledge and understanding of the main principles and concepts of the Quality part of the Common Technical Document.

HOW WE WORK TOGETHER TO ENSURE (EARLY) ACCESS TO MEDICINES

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.

Online conference. This training course is intended for both manufacturers and distributors of medical devices/ in vitro medical devices and will address various questions/issues under the MDR/IVDR.

Join us for our fourth session on the “Sources of life sciences regulation”.