How to save time managing Agency correspondence with AI

Health authority questions are coming faster — and in greater volume — than ever before. For regulatory teams, that means more correspondence to process, less time to respond, and mounting pressure to keep critical therapies moving through review.

In this webinar, we’ll explore how AI can ease the burden by automatically capturing agency correspondence, extracting key questions and commitments, and even assisting in drafting responses. You’ll discover how regulatory teams can reclaim valuable time, reduce manual effort, and improve consistency — all while accelerating turnaround times for approvals.

Join us to learn how Ennov’s AI-powered approach is helping life sciences companies stay ahead of regulatory demands without burning out their teams.

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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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