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Jan 9, 2023
5 min read
Considerations When Evaluating eCTD Submission Publishing and Management Vendors
Getting your product’s regulatory submission ready to send to the FDA, Health Canada, or European health authorities can be...
Feb 21, 2022
1 min read
eCTD Module 1 Specification Reminder
O March 1, 2022, the US FDA will no longer be accepting the eCTD Module 1 specification v1.3 (US regional DTD v2.01)
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