How to Move from TMF Workarounds to True Compliance

Are you still using spreadsheets, shared drives, or Word documents to manage your Trial Master File? Struggling to maintain compliance, oversight, or alignment with your CTMS and EDC? 

It might be time to rethink your approach. 

In this 30-minute session, we’ll walk through how life sciences organizations can modernize their TMF processes with a dedicated, ready-to-use eTMF that ensures compliance, improves visibility, and sets the foundation for seamless integration with your CTMS and EDC. 

You’ll learn: 

  • What to look for in a true eTMF solution 
  • Why Excel, PDFs, and shared folders put compliance at risk 
  • How a connected platform improves data capture and trial oversight 
  • How to move quickly without sacrificing flexibility or control 

Whether you’re just getting started or already managing trials at scale, this session will give you practical steps to simplify documentation, reduce risk, and drive trial efficiency, without a massive system overhaul. 

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More than 450 Life Sciences companies around the world are powered by Ennov

“It's quite simple – the week we went into production, we had cleared our schedules to answer support calls. Waiting by our phones, we received no calls and wondered if people were actually working. Well, yes, they were indeed working, but they just didn't need help!
François Faivre
François FaivreIT Project Director
“What sets Ennov apart is the unified database. You could integrate your eTMF with your clinical database and submission documents because the data is all in one place.”
Jakob Juul Rasmussen
Jakob Juul RasmussenFounder and Managing Director
“Last year, our team needed to pull historical data on submissions in the US. It took our entire team one full week to identify and assemble the necessary information. With Ennov RIM, we will now be able to do this in 10 minutes or less. Ennov RIM truly is a one-stop shop for our needs.”
Jamie Brugnano Sr
Jamie Brugnano SrManager, Regulatory Affairs
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