Effective Training management powered by AI
Proving training records to regulatory authorities? Our AI-powered solution automatically generates compliance assessments from your documentation—no more manual effort, just click and go!
What’s In It for You?
📝 Auto-Generated Assessments: Seamlessly align with FDA, EMA, and ICH—no more manual quiz-building.
✅ Zero Guesswork: Instantly document proof of competency for regulatory scrutiny.
🔍 No More Audit Anxiety: Easily demonstrate how your teams meet global health authority expectations.
⏰ Time Back in Your Day: Trade red tape for real innovation (or a well-deserved coffee break). ☕
Discover it all in the webinar recording.
Become a Member of the Ennov Community
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!
“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.”
“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.”
Explore Success Stories from Ennov Users.
Effective Regulatory Information Management can be complex. Your software shouldn’t be.
Effective Regulatory Information Management can be complex. Your software shouldn’t be.
From Days to Minutes: How Bachem Streamlined their Regulatory Submission Process
Discover how Ennov helped revolutionize their regulatory data management, saving valuable time and resources.
Discover how Ennov helped revolutionize their regulatory data management, saving valuable time and resources.