Navigating from CTD to eCTD in Brazil

US FDA Adopts ICH Clinical Trials Guideline with Exclusive Reference to E2B(R3) Standards

CMDh Updates Guidelines to Implement Northern Ireland Protocol (Brexit relevant information)

US FDA announces that DTD version 3.3 will be made mandatory for eCTD submissions

Use of E2B(R3) Becomes Mandatory June 2022 - How to Prepare

EU Clinical Trials Regulation Now in Effect

EMA Updates Technical Guidance for eCTD Submissions in the EU

MHRA updates Guidance for Centrally Authorized Products (CAPs) to UK Marketing Authorization (MAs)

New EU Guidance on Data Submission for Investigational Medicines

Australia readies itself for eCTD only

China NMPA will be accepting eCTD submissions from 29th December 2021

Gens & Associates IDMP Vendor Assessment & Capability Survey - How does MPDmanager powered by CARA compare to competing products?

The FDA’s OPDP eCTD is now in effect - what does it mean for you?