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# Highest-ever Electronic Submissions at CDER
- URL: https://www.fdaweb.com/highest-ever-electronic-submissions-at-cder/
- Published: 2016-03-09T12:00:00.000Z
- Updated: 2026-09-15T02:42:11.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5135013

> An electronic submissions update at a recent DIA regulatory submissions, information, and document management forum indicated that there were 14,700 electronic submission gateway submissions to CDER in 12/2015, making it the highest month ever for electronic submissions. CDER Division of Data Management Services and Solutions director **Ginny Hussong** also [said](http://www.fda.gov/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/ucm229642.htm?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery) that more than 1,600 new Module 1 submissions had come in as of 2/1/15\. Electronic submissions include 88% of study data submitted in support of new NDAs.  
>  
> Hussong reminded attendees that 5/5/17 is the deadline for required eCTD submissions for NDAs, BLAs, ANDAs, and DMS, while 5/5/18 is the deadline for commercial INDs. Paper and non-eCTD submissions will no longer be accepted after those deadlines.  
>  
> Other FDA presentations (linked from above link) included an eCTD validation update and global identification of medicinal products.