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Titre

Pharmaceutical Regulatory Affairs: an Introduction

Dates

04.10.2019 (13-17h) 18.10.2019 (13-17h) 01.11.2019 (13-17h) 15.11.2019 (13-17h) 29.11.2019 (13-15h) 13.12.2019 (13-15h)

Lang EN Workshop language is English
Organisateur(s)
Intervenant(s)

 

Pierre Humbert-Droz, Pharmacist, PhD from School of Pharmaceutical Sciences, University of Geneva, with a broad experience in R&D and Regulatory Affairs in international companies such as Novartis Consumer Health, currently consultant for GSK Consumer Healthcare.

 

 Géraldine Bouvier, Pharmacist, MSs from University of Pharmacies of Paris and Lille, with a deep experience in Regulatory Affairs, having worked for Health Authority & international companies (such as Novartis Consumer Health & currently GSK Consumer Health).

Description

 

The objective of this course is to give an overview of the worldwide regulatory environment and regulatory requirements governing the pharmaceutical industry. It will provide an understanding of this dynamic discipline which combines science & regulations and offers large opportunities for interesting careers at the interface between pharmaceutical company's various departments. It will describe the regulatory environment in the major regions of the globe to support development of new products to obtain marketing authorizations. This course will also provide an introduction to the lifecycle management, focusing on drug products & medical devices together with considerations on trends and future within the pharmaceutical industry.

Lieu

CMU, room B09.2125A, 9th floor

Information
Places

15

Délai d'inscription 30.09.2019
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