1 Day Mastering Generic CTD Submissions in the MENA Training Course: Specific Documentation and Study Requirements Essential for Successful Submissions (ONLINE EVENT: May 19, 2026)

Explore opportunities in mastering MENA's generic CTD submissions with expert-led insights. Harness regional expertise to streamline processes, minimize delays, and align with global strategies for ...
RAPS

FDA Unveils New Changes to eCTD Submission Formats

If you weren't paying attention closely late last week, you might easily have missed a small but important announcement made by the US Food and Drug Administration (FDA). By the end of 2014, it says, ...
RAPS

'Major Updates' to eCTD Module 1 Released by FDA

The US Food and Drug Administration (FDA) has announced the release of "major updates" to Module 1 of the electronic common technical documents (eCTD), used to supplement all eCTD submissions in the ...