Ennov
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Ennov QMS ensures the highest degree of traceability, knowledge sharing and compliance throughout your company.
Easily design and capture multi-centric clinical study data with a single comprehensive software
Easily design and capture multi-centric clinical study data with a single comprehensive software. EDC software significantly streamlines randomization, study design, consistency tests, medical coding (MedDRA, WHO Drug), data import and export. You can design your own eCRF without any IT skills thanks to our graphical CRF creation tool.
Ennov Process allows you to automate your Quality processes and enforce the activities, participants and traceability required by your SOPs using our visual form builder and graphical workflow modeling utilities. Ad hoc processes or those that remain stalled for months are a thing of the past.
Ennov RIM is a comprehensive Regulatory Information Management (RIM software designed to help organizations efficiently manage product details, registrations, submissions, and regulatory activities. It seamlessly integrates with Ennov Doc and Ennov Dossier, providing a unified platform for regulatory operations. The software is fully configurable to support an organization's entire product portfolio, ensuring adaptability to various regulatory requirements. Ennov RIM offers workflow-driven process automation, robust data querying, reporting, and visualization capabilities, and ensures full compliance with xEVMPD submissions. Key Features and Functionality: - Comprehensive RIM Solution: Provides a holistic approach to managing regulatory information across the product lifecycle. - Seamless Integration: Intrinsically connected with Ennov Doc and Ennov Dossier for streamlined document and dossier management. - Full Configurability: Adaptable to support the entire product portfolio, accommodating various regulatory requirements. - Process Automation: Utilizes workflow-driven automation to enhance efficiency and reduce manual tasks. - Advanced Data Management: Offers robust querying, reporting, and visualization tools for insightful data analysis. - Regulatory Compliance: Ensures full compliance with xEVMPD submissions, meeting stringent regulatory standards. Primary Value and User Benefits: Ennov RIM addresses the complexities of the global regulatory landscape by providing a centralized and integrated platform for managing regulatory information. It enhances operational efficiency through automation, reduces the risk of non-compliance, and offers valuable insights through advanced data management tools. By supporting the entire product portfolio and ensuring compliance with evolving regulatory requirements, Ennov RIM empowers organizations to navigate the regulatory environment effectively and maintain a competitive edge.
Retrieve your documents faster. Collaborate effectively - 100% web-based. Manage document lifecycles from creation through approval and archive.
A Comprehensive Solution to Capture and Manage Clinical Trial Information. The Ennov Clinical suite consists of Clinical Data Management applications (EDC, RTSM and ePRO) as well as Clinical Trial Management applications (CTMS and eTMF) that are available for deployment in the cloud or on premises
Atrium can provide indicators for many fields of activity: regulatory issues, finance, quality, sales, marketing,
Ennov Reviews
Maxime E.
PharmacistEnnov Quality
Victor S.
Administrateur Systèmes Qualité Informatisés Groupe | Data AnalystReview on Quality Management System (eDOC, eProcess, eTraining)
Anand P.
Good Software to manage large sample clinical trials
About
Ennov | The only AI-powered unified compliance platform to support the entire product life cycle
With offices in the US, UK, Europe, and Asia, Ennov provides the most original, comprehensive and cost-effective suite of software solutions for the Life Sciences industry. From leading pharmaceutical companies to emerging biotechs, we proudly serve over 450 companies and 500,000 users around the world.
