Unified QMS and RIM
Learn how Ennov RIM enables the effective management of CMC variation change controls.
Learn how Ennov RIM enables the effective management of CMC variation change controls.
Learn best practices for migrating documents from legacy systems into Ennov.
Learn how Ennov CTMS and eTMF enables planning, management, documenting of clinical trials.
Learn how Ennov RIM enables the management and submission of XEVMPD information to the EMA.
Learn how Ennov enables compliance with the US FDA’s 21 CFR Part 11 guidance.
Learn about the interactions between eDMS and IDMP to gain insights into the best practices regarding data governance and IDMP compliance.
Learn how Ennov Doc’s integration with Office 365 drives innovation through collaborative authoring.
Learn the key areas where a unified CTMS and eTMF can result in the greatest benefit.
Learn how to achieving Regulatory Operational Excellence through unified Quality and Regulatory information management..
Learn how Ennov training automates the training of staff on corporate policies and procedures to keep training records up-to-date.
Learn how Ennov Process can automate business processes to streamline business operations, ensure compliance and increase efficiency.
Learn how PV-Signal Manager can help with the prioritization, evaluation, classification and review of safety signals.
Learn how PV-Analyzer can help prepare statistical detailed analyses of safety data to reduce risk.
Learn how PV-Works Vet can help with the collection, management, reporting and evaluation veterinary safety data.
Learn how PV-Works Human can help with the collection, management, reporting and evaluation patient safety data.
Learn how Ennov EDC facilitates complete and accurate data collection and improves communication within clinical teams.
Learn how Ennov eTMF provides all the functionality required to effectively and efficiently manage your clinical trial documentation.
Learn how Ennov CTMS can help with the planning, management and reporting of clinical trials.
Learn how Ennov RIM can help streamline regulatory processes and improve data quality.
Learn how Ennov Dossier helps meet Regulatory submission publishing challenges.
Learn how Ennov Doc can help meet Regulatory document management challenges.
Learn why effective management of Clinical CAPAs is key to operating in a state of control.
Learn why an optimized TMF strategy is essential to maintaining inspection readiness and reducing risk.
Learn how Vetoquinol implemented Ennov Doc and Ennov QMS to reduce compliance risk and improve performance.
Implementing an electronic document, business process and training management solution to increase efficiency across the organization.
Utilizing Ennov PV to drive drug safety outsourcing services to pharmaceutical companies.
Learn how GEFCO implemented Ennov Doc to realize productivity gains within their Quality organization.
Leveraging Ennov Clinical to transform business by delivering Clinical data management services and increasing revenue.
Aligning regulatory activities to strengthen competitive position.
Learn how Maincare is leveraging Ennov Doc and the Ennov REST API to include document management capabilities in their products.
Ennov announces its inclusion in the “2020 World Class RIM Whitepaper; Is Industry at a Performance Tipping Point”, published by Gens & Associates, a leading
Ennov announces its inclusion in the 2020 “Market Guide for Quality Management System Software”, published by Gartner, Inc., the leading information technology research and advisory
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