Best Practices Creating IND,ANDA Electronic Submissions for US FDA
【Webinar invitation】Best Practices Creating IND,ANDA Electronic Submissions for US FDA
Hello,
efficiently managing validated and compliant IND / ANDA submissions for US FDA can be challenging. Using EXTEDO’s eCTD management software solution eCTDmanager, you can easily build, view, validate and publish IND / ANDA submissions as well as other submission types based on eCTD, NeeS, Paper, and other regional formats around the world. Ensure effortless compliance by using the same validation technology as 35 regulatory authorities worldwide!
EXTEDO & GGA invite you to their complimentary webinar “Best Practices Creating IND / ANDA Electronic Submissions for US FDA”
During the webinar Ralf-Peter Berg will talk about best practices creating eCTD submissions and give you a live demonstration of how to effortlessly create an IND / ANDA submission within eCTDmanager.
Event Details and Registration
Date: Thursday, 08 August 2019
Time: 03:00 pm CST (Taipei)
09:00 am CEST (Madrid, Berlin)
Duration: 60 Minutes
Participation is free of charge. “
Registration:
https://attendee.gotowebinar.com/register/3430276568049167373
Contact person: 02-2795-1777 ext.3029 Vicky