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?
OMS to become mandatory for all submissions to EMA
The Mystery of the EU IG - Insider Perspective
EXTEDO to extend its EXTEDOpulse RIM software solution using Generis’s CARA™ foundational content & business process management platform
EXTEDO Donates Laptops to Disadvantaged Children for Homeschooling
Implementation of the new Veterinary Medicines Regulation
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