EMA Updates Technical Guidance for eCTD Submissions in the EU
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MHRA updates Guidance for Centrally Authorized Products (CAPs) to UK Marketing Authorization (MAs)
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New EU Guidance on Data Submission for Investigational Medicines
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Australia readies itself for eCTD only
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China NMPA will be accepting eCTD submissions from 29th December 2021
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Gens & Associates IDMP Vendor Assessment & Capability Survey - How does MPDmanager powered by CARA compare to competing products?
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The FDA’s OPDP eCTD is now in effect - what does it mean for you?
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OMS to become mandatory for all submissions to EMA
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The Mystery of the EU IG - Insider Perspective
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EXTEDO to extend its EXTEDOpulse RIM software solution using Generis’s CARA™ foundational content & business process management platform
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EXTEDO Donates Laptops to Disadvantaged Children for Homeschooling
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Implementation of the new Veterinary Medicines Regulation
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