Understanding European Filing and Registration Procedures for Drug Approval 2016
16 Nov 2016
Webinar
Description
Topics
Steps required prior to submission of a marketing authorization application (MAA)
How to choose the appropriate pathway to drug approval in the EU
Expectations of the sponsor during the review process
Key timelines before, during, and after submission of an MAA
Life cycle management of the MAA
Follow up on applications after approval
Who should Attend
Employees involved in any area providing information for a MAA
Vice Presidents, Directors, & Managers of regulatory, clinical and manufacturing areas
All companies developing drugs or biologics for approval in the EU
All Regulatory affairs personnel working on EU submissions
Past Events
Understanding European Filing and Registration Procedures for Drug Approval 2016 - 16 Nov 2016, Webinar (63469)
Important
Please, check "Understanding European Filing and Registration Procedures for Drug Approval" official website for possible changes, before making any traveling arrangements
