Boehringer Ingelheim
selects the Ennov platform for
Regulatory information Management (RIM)

A unified content and information management platform to support the entire Life Sciences product development continuum

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Our comprehensive QMS improves operational efficiency and ensures regulatory compliance

clinical software suite


Our total solution for capturing and managing Clinical Trial information streamlines
clinical operations

regulatory software suite


Our world-class Regulatory content and information management software accelerates HA approvals

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Our end-to-end solution for collecting, reporting and analyzing human and vet PV data minimizes risk

event commercial regulatory


Our complete management of professional events ensures DMOS, EFPIA, HCP and COI compliance

More than 150 Life Sciences companies around the world use Ennov

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"We don't have to spend time searching for documents. Everything is stored and organized in the same place and accessible from anywhere at any time."

Regulatory Operations Director, Septodont

Download Septodont's Case Study

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For more than 19 years, Ennov has been developing innovative, powerful and easy-to-use software for document and process management.

Using the knowledge and best practices gained from more than 150 Life Sciences customers and over 500 total customers, Ennov has designed and built solutions specifically for the health and life sciences sectors: Quality, Pharmacovigilance, Clinical Operations and Regulatory Affairs.

Ennov Compliance Platform

Unified Document Management, Business Process Management, Business Intelligence and Learning Management

Ennov solutions are built on our Unified Compliance Platform which is designed specifically for the management of regulated content and processes.
The Ennov platform is the technological foundation of our Regulatory (EDMS, Dossier Publishing, RIM, IDMP), Quality (EDMS, QMS) and Clinical (eTMF and CTMS) solutions.

Our platform approach provides significant advantages over other products on the market:

  • Meets the regulatory needs of life sciences organizations
  • Complies with 21 CFR part 11
  • Is open to integration with other systems via its REST API
  • Is flexible and easy to configure
  • Incorporates unified ergonomics that are consistent throughout the software suite
  • Presents modern user experience and at the forefront technical innovation

What's happening at Ennov

Download our insightful White Papers


Ennov to Exhibit at the 2019 RAPS Regulatory Convergence


Ennov to Exhibit at the 2019 DIA Global Annual Meeting, June 23-27 in San Diego, CA


Ennov to Exhibit at the 2019 DIA RSIDM Forum

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