Qdossier presenting on Biosimilars

On October 11 and 12th, Qdossier will present a 2-day training course which is part of the Management Forum training curriculum. The interactive course will cover the regulatory pathways and challenges for biosimilars in both the US and EU and the regulatory strategies and requirements for development of biosimilar products. During this training you will:

• Discuss global considerations and definitions of biotech/biosimilar products
• Gain an invaluable overview of the regulatory pathways for biosimilars in the EU and US
• Understand the key Module 3 dossier requirements for biotech products versus pharmaceutical products
• Learn how to develop effective strategies for development of biosimilar products

Find more information on the event here

Speaker: Marloes van der Geer & Hans van Bruggen