eCTD Format

August 28, 2023
Medicinal Products,
Publishing and Submission
The USFDA’s Game-changing Guidance on Electronic Submissions for Promotional Materials and Grouped Submissions
June 20, 2023
Medicinal Products,
Publishing and Submission
Fast-track eCTD Submissions in Australia
May 5, 2023
Medicinal Products,
Publishing and Submission
eCTD v4.0 Requirements for Non-EU Countries in Europe
May 2, 2023
Medicinal Products,
Publishing and Submission
eCTD Validation Criteria Version 2.1 in China: What You Need to Know!
September 27, 2019
Medicinal Products,
Publishing and Submission
Health Canada Mandates eCTD Format - For Type I, II, III, IV Master File Submissions
May 25, 2017
Medicinal Products,
Publishing and Submission
eCTD in Limelight: Should HC Electronic Submissions be your Next Focus?
April 19, 2017
Medicinal Products,
Regulatory Affairs
FDA Deadline Extension for Master Files and The Motto Behind
April 13, 2017
Medicinal Products,
Publishing and Submission
ANDA first-cycle approvals and the need for eCTD
April 7, 2017
Medicinal Products,
Publishing and Submission
eCTD in Limelight. HPRA to Make Electronic Submissions Mandatory
April 4, 2017
Medicinal Products,
Publishing and Submission
FDA eCTD Deadline – Benefits and the Approach
February 28, 2017
Medicinal Products,
Publishing and Submission
Application Types for FDA’s Upcoming eCTD mandate
January 17, 2017
Medicinal Products,
Publishing and Submission
EMA eSubmission Roadmap: Your guide to future MA application format requirements