EMA Labelling and Packaging Regulations
Introduction The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU) in charge of scientific evaluation, regulation, and quality control of
EU Marketing Authorization Procedures
European Medicines Agency The European Medicines Agency (EMA) is responsible for the scientific evaluation of centralized marketing authorization applications (MAA’s). A marketing authorization (MA) is the authorization
Webinar: Advanced Therapy Conundrum: Should You Build, Outsource, or Go Hybrid?
Webinar: Advanced Therapy Conundrum: Should You Build, Outsource, Or Go Hybrid? June 22, 2021. 2:00PM EST/ 7.00PM GMT Companies developing advanced therapies have to decide
