Ennov Doc for Pharmacovigilance

Centralize your PV documentation in one compliant system

Document Management for PSMF, Agreements, and Risk Documentation

Stay inspection-ready with a single 21 CFR Part 11–compliant system of record

Teams often manage the Pharmacovigilance System Master File (PSMF), documents, and partner agreements across shared drives, email, and disconnected tools. That fragmentation leads to version confusion, slow retrieval, limited traceability, and gaps in oversight of safety obligations, increasing inspection risk and making it harder to stay audit-ready across EU and US requirements.

Ennov Doc for PV centralizes documents and the PSMF, while supporting agreement management in a structured repository built for compliance. Teams can maintain an inspection-ready PSMF, control document lifecycles, and track agreements, obligations, and related activities with clear ownership and audit trails supporting 21 CFR Part 11. The result is more consistent global documentation, secure collaboration across internal and partner teams, and fewer operational gaps when audits and inspections occur.

The 4 Key Components of Ennov Doc for PV

Submissions & Reports

Centralize all submissions and reports—aggregate, clinical, and safety—generated from your safety database and submitted to Health Authorities and other competent bodies, fully aligned with global reporting requirements.

Risk Management​

Manage the complete lifecycle of global and local Risk Management documents, leveraging safety data, risk assessments, and quality metrics to support continuous and robust benefit–risk evaluation.

Agreements

Streamline the management of agreements defining roles, responsibilities, data exchange, and obligations across partners, affiliates, and third parties. Track responsibilities with advanced search, workflows, task management, and automated due-date notifications to ensure operational oversight. ​

Pharmacovigilance System Master File (PSMF)

Aggregate and maintain all documentation required under GVP Module II and Directive 2001/83/EC / Regulation (EC) No 726/2004 within a structured binder. Automatically generate an audit-ready PSMF that clearly documents your system structure, processes, and regulatory compliance.

Core Capabilities

Key Features

An End-To-End Solution for Collecting, Reporting and Analyzing Human and Vet PV Data 

The Ennov Pharmacovigilance solution keep the collection, management, assessment, and reporting of human or veterinary adverse events in one unified database while also providing advanced signal detection and PV data analysis tools.

Why Choose Ennov

Over 500,000 users trust Ennov

Providing you freedom of choice

Cloud-based or On Premises

Multi-Platform

ISO 9001 & 27001 Certified

How can we help you?

Fill out the form and we'll be in touch.