Navigating from CTD to eCTD in Brazil

Implementation expectations of eCTD 4.0

Key Concepts Behind eCTD 4.0 and their Impact on Product Submissions

The Drivers and Benefits behind eCTD 4.0

The EMA prepares itself for Brexit

The Chinese Food & Drug Administration moves to eCTD

EMA Officially Endorses the New EudraVigilance System for Adverse Reactions

Why we believe in IDMP, and you should too

EXTEDO Opens New Office in Shanghai

EXTEDO上海分公司成立！

Health Canada confirms mandatory use of eCTD format from 1st January 2018

eRA 2017 - A first-timers impressions

Overview of the New Requirements for Electronic Submission of Drug Master Files (DMFs)