USFDA will host a webinar and Q&A Session on “How to use CDER Direct to submit Registration and Listing Structured Product Labeling (SPL) files”.

On Tuesday September 16, 2014 at 1:00 pm EDT, CDER SBIA will host a webinar and Q&A session entitled “How to use CDER Direct to submit Registration and Listing Structured Product Labeling (SPL) files”. This webinar will provide a brief demo of CDER Direct, a new software application to assist companies in submitting drug registration and listing submissions.

  

To register for this Event, please go the following link: https://collaboration.fda.gov/sbia0916/event/registration.html

(Registration password needs to be 8 characters and alphanumeric)

Note: Your registration acknowledgement will include the webinar access link. 

Audio will broadcast from your computer speakers. Please mute your microphones (to reduce audio feedback) during the webinar.

Closed captioning will be provided.

Please note: There is a user capacity limit for this webinar. For those who cannot enter the webinar, please know that it will be recorded and a link will be posted to this page:  

http://www.fda.gov/Drugs/DevelopmentApprovalProcess/SmallBusinessAssistance/ucm070334.htm

Questions/Comments can be submitted live via a Q/A chat window.

For questions concerning the webinar, please contact CDER SBIA at:  (866)-405-5367 | (301)-796-6707 

CDER SBIA webinar series: http://www.fda.gov/Drugs/DevelopmentApprovalProcess/SmallBusinessAssistance/ucm070334.htm