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How AI Can Support Your Organization’s ePI Implementation
ePI Readiness Takes More Than One System
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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 extends 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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New Guidance on Handling of DCP/MRP
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EXTEDO continues community outreach - sponsors local ski club
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Therapeutic Goods Administration (Australia) to transition all regulatory submissions to eCTD-only, starting in 2021
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MHRA Publishes New Guidance for Converting Centrally Authorized Products to UK Marketing Authorizations
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