eCTD Submissions, or electronic Common Technical Document Submissions, refer to the electronic format for submitting regulatory information to health authorities. The eCTD format was developed as ...

The EMA has now reinforced its commitment to electronic submissions by mandating the use of the eCTD format for the centralized procedure of all electroniconly submissions. "From here on in, noneCTD ...

The eCTD has increased efficiency for reviewers and improved submission times. This two day workshop will provide you with an in-depth review of the content and format requirements of the CTD/eCTD.

WARNER ROBINS, Ga. , Oct. 21, 2014 /PRNewswire/ — Today in Atlanta, GA , Aquila Solutions, LLC announced the immediate availability of eCTD Accelerator – Templates, enabling sponsors and consultants ...

Ultimately geared to establishing the Electronic Common Technical Document (eCTD) as the required format for electronic submissions, the implementation strategy is being pursued within the wider ...

The original deadline for submitting Type III DMFs in eCTD format was May 5, 2017; however, that deadline was extended for an additional 12 months and subsequently pushed back again to May 5, 2020 ...

Regulators at Health Canada have announced the finalization of guidance intended to assist sponsors in preparing electronic common technical documents (eCTDs) to submit their pharmaceutical dossiers ...

The DRAC team has been working to train themselves on how to prepare, publish, and view submissions in an electronic format since eCTD became operational.

Dublin, June 27, 2024 (GLOBE NEWSWIRE) -- The "eCTD Submissions - Fundamentals and Process" training has been added to ResearchAndMarkets.com's offering.eCTD Submissions, or electronic Common ...