Managing Electronic Drug Master File Submissions

Описание к видео Managing Electronic Drug Master File Submissions

FDA discusses information to manage a DMF in eCTD format, including electronic submission requirements, metrics, best practices, frequently asked questions, and where to obtain help.
Presenter:
Jonathan Resnick, Division of Data Management Services and Solutions, CDER

Learn more at: https://www.fda.gov/drugs/news-events...
-------------------- 
FDA CDER’s Small Business and Industry Assistance (SBIA) educates and provides assistance in understanding the regulatory aspects of human drug products & clinical research.  

Upcoming Training - https://www.fda.gov/cdersbia
SBIA Listserv - https://public.govdelivery.com/accoun...
SBIA 2021 Playlist -    • 2021 CDER Small Business and Industry...  
SBIA LinkedIn:   / cder-small-business-and-industry-assistance  
SBIA Training Resources - https://www.fda.gov/cdersbialearn
Twitter -   / fda_drug_info  
Email - [email protected]  
Phone - (301) 796-6707 I (866) 405-5367

Комментарии

Информация по комментариям в разработке