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 ...

Dublin, Aug. 01, 2023 (GLOBE NEWSWIRE) -- The "Filing eCTD Submissions Training Course" conference has been added to ResearchAndMarkets.com's offering. This intensive one-day course will provide an ...

In 2005, the heads of the European medicines agencies agreed that all EU member states must have the infrastructure and processes in place to handle only electronic Common Technical Document (eCTD) ...

All regions that have published guidelines will mandate implementation of eCTD version 4.0 by 2028, with more regions to follow in the future Developed by the International Council for Harmonisation ...

The European Medicines Agency (EMEA) has set a timetable for the implementation of electronic-only applications for marketing authorisation through the centralised approvals procedure. The European ...

HORSHAM, Pa., July 18, 2023 /PRNewswire/ -- LexisNexis® Reed Tech, a leading provider of regulatory submissions, data management and analytics solutions for the life sciences industry, is expanding ...

With an approaching deadline of 1 January 2019, Health Canada is requesting industry input on establishing mandatory requirements for submitting drug master files (DMFs) using the electronic common ...

This intensive one-day course will provide an overview of eCTD submissions and clarify the main components required for successful submission. The expert speakers will share their practical ...