Place : Spain, Madrid
Contact Person:Andrea Weber
Description:Understand the specific regulatory & legal environment concerning generic medicinal products. Update your knowledge on regulatory procedures for new applications and variations. Get an overview on the documentation for Generic applications. Understand the current integrated life-cycle approach from development to registration and maintenance, including ICH Q12.
Deadline for abstracts/proposals : 3rd June 2020
Organized By :Fleming.
Keynote Speakers : Dr. Helmut Vigenschow
Conference Highlights :Marketing Authorisation Procedures in the EU, Development challenges of Generics, Structure and content of the regulatory documentation
Check the event website for more details.