December 4, 2017
2:00PM - 4:00PM (Eastern)
This event is FREE
View Agenda: Click Here
The Food and Drug Administration, Center for Drug Evaluation and Research and Small Business and Industry Assistance (CDER SBIA), welcomes you to our webinar series.
These events focus on a specific topic and provide an opportunity for small business and industry entities to learn more about the FDA and basic drug regulation. The webinars support CDER SBIA’s mission of promoting productive interaction with regulated industry by assisting small pharmaceutical business and industry with information relating to the development and regulation of human drug products.
CDER invites you to our LIVE webinar:
REMS Integration Initiative: An Overview
to be held on December 4th from 2:00pm – 4:00pm (Eastern).
Join us as our FDA experts present on the recently concluded REMS Integration Initiative. We will also introduce the new REMS document template and provide an update on REMS SPL and the REMS@FDA website.
You will have an opportunity to submit questions during a live Q and A session after the presentation.
This webinar has been pre-approved by RAPS as eligible for up to 1.5 credits towards a participant’s RAC recertification upon full completion.
Please note that the credit is only available for participation in the live
event and not for watching the recording afterwards.
For questions concerning the webinar, please contact CDER SBIA at:
(866) 405-5367 | (301) 796-6707
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