The Eurasian Union (EAEU) is working to implement a submission process that is similar to the eCTD model and also other ICH guidelines. The new regulation affects all marketing authorization holders as well as all new drug applications. This webinar is a must-see for anyone who wants to stay up-to-date and implement the new requirements smoothly.
Proud to bring inspirational speakers from across the globe.
Director, Principal Consultant Regulatory Operations Industry / Agency Liaisons
Independent Consultant, Regulatory Affairs and eSubmission Specialist Independent Consultant