Information détaillée concernant le cours

[ Retour ]
Titre

Pharmaceutical Regulatory Affairs: an Introduction

Dates

Friday 2 october, 10:00-12:00; Friday 16 october, 10:00-12:00; Friday 23 october, 13:00-15:00; Friday 6 november, 13:00-15:00; Friday 13 november, 10:00-12:00; Friday 20 november 10:00-12:00;Friday 27 november, 10:00-12:00; Friday 4 december, 10:00-12:00; Friday 11 december, 08:00-12:00 (4 hours session)

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

Dr Géraldine Bouvier, Director Global Regulatory Affairs, GSK Consumer Healthcare (Ex Novartis Consumer Health SA Nyon); Dr Pierre Humbert-Droz, Regulatory Affairs, CMC Expert Consultant (MITC SA) / GSK Consumer Healthcare (Ex Novartis Consumer Health SA Nyon)

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

Visioconferences due to COVID-19

Information
Places

12

Délai d'inscription 25.09.2020
short-url short URL

short-url URL onepage