Ennov RIM
Regulatory information management at global organizations is rarely integrated and usually consists of collections of spreadsheets, homegrown databases, emails and ad hoc reports – each full of redundant and/or inconsistent data. Ennov RIM is a purpose-built application for the management and tracking of therapeutic product details, registration information and regulatory processes.
How to Accelerate Content Preparation with AI (Powered by DocShifter)
If you’re still spending hours manually bookmarking, hyperlinking, or reformatting documents before submission, this session is for you. Discover how DocShifter can incorporate powerful new
AI in Regulatory: Agents, Answers, Action!
Welcome back to the Ennovation Podcast, where we bring you the latest trends, insights, and expertise in life sciences and regulatory affairs. This time, we’re joined by Steve Gens, founder of
IDMP Readiness in 2026: How to avoid last minute panic | by Ennov & NNIT.
IDMP deadlines are approaching fast, June 2026 and December 2026 will force many organizations to turn “regulatory data” into structured, reusable IDMP-ready data. The challenge
Implementing AI in Regulatory: Key Considerations for Success
This practical session showcases a clear and realistic approach for evaluating and implementing AI solutions in the pharma/device regulatory space. You’ll learn how to set
eCTD 4.0 Pilots: Cleared for Takeoff!
Welcome back to the Ennovation Podcast, where we bring you the latest trends, insights, and expertise in life sciences and regulatory affairs. This time, I’m joined by Diarmuid Waide, Regulatory Product
Ennov IDMP EASI Connector for RIM Integration
Meeting the EMA’s IDMP requirements is critical, but it doesn’t have to be complicated. Ennov’s powerful automated solution simplifies PMS data enrichment, saving you time