Is Your Portfolio Ready for Data Enrichment?
The EMA has taken a huge step towards IDMP implementation with the go live of the Product Management Service (PMS) and integration of PMS data
February 18, 2025
eCTD 4.0 & Medical Devices: What’s Happening in 2025?
Welcome to the Ennovation Podcast, where we bring you the latest trends, insights and expertise in life sciences and regulatory affairs. For the first episode,
February 14, 2025
eCTD 4.0: Key Milestones
eCTD 4.0 is one of the main focal points of the regulatory world and there has been significant progress over the last year, with some
February 13, 2025
MHRA consider dramatic changes to the regulation of medical devices and in vitro diagnostics
The MHRA recently closed their consultation on routes to market for medical devices and in vitro diagnostic devices. The consultation, which closed on 5 January
February 12, 2025
eCTD 4.0 Pilot Readiness Checklist
eCTD 4.0 is one of the main focal points of the regulatory world, and participating in an eCTD 4.0 pilot is a great opportunity to get experience with the future of regulatory submissions. Make sure you’re prepared and get the most out of your pilot experience!
February 12, 2025
Ennov Training
Streamline Training with a Learning Management System. Simplify compliance monitoring, evaluate staff proficiency, automate onboarding.
February 7, 2025
Register to access to our exclusive library!
- White Papers
- Case Studies
- Product Demos
- Industry Briefs
- and more...
Highlight Post
Recent Posts
Artwork Management Made Easy (w. practical examples)
March 28, 2025
How to Save Time Managing Agency Correspondence with AI
March 7, 2025
Effective Training Management Powered by AI
March 7, 2025
Ennov to Sponsor the 2025 DIA RSIDM Forum
January 16, 2025
Introducing Ennov 10.3
December 3, 2024
Ennov and CognifAI Partner for AI-Driven Pharmacovigilance
October 10, 2024