Clinevo Literature Automation

Clinevo Literature Automation is a cloud-based software tool designed for pharmacovigilance teams in life sciences, pharmaceutical, biotech, and CRO organisations. It automates the search, retrieval, screening, and management of scientific literature from multiple sources, reducing manual effort and supporting regulatory compliance throughout the literature review process.

The platform integrates with established pharmacovigilance databases and provides analytics dashboards for safety signal detection, making it applicable to drug safety teams that need to manage large volumes of scientific publications and research findings efficiently.

Automated Retrieval and Screening

• Auto-searches and retrieves literature from PubMed, EMBASE, regulatory databases, clinical trials registries, and journals.
• Categorises, tags, and prioritises literature based on drugs, adverse events, or regulatory relevance.
• Automates collection, screening, and analysis of scientific literature to reduce time spent on manual processes.

Integration with Pharmacovigilance Databases

• Pushes finalised articles directly into PV databases including Argus, ArisG, and Clinevo Safety.
• Supports end-to-end workflow management from initial literature retrieval through to final reporting.

Compliance, Audit, and Accuracy

• Tracks literature reviews, documents decisions, and maintains audit trails to support regulatory compliance.
• Automated processes reduce human errors, keeping literature data accurate and audit-ready.
• Tracks and documents literature review activities to help teams stay aligned with evolving regulations.
• Complies with 21 CFR Part 11, Annex 11, GxP, and GDPR standards, supporting regulatory inspection readiness.

Real-Time Monitoring and Reporting

• Provides customisable analytics dashboards and reporting tools for identifying safety signals and trends.
• Dashboards offer real-time tracking of literature compliance, quality, and workflow performance.
• Supports real-time collaboration, integration, and reporting across teams.

Accessibility and Interface

• Accessible on any device via internet or intranet, with support for Internet Explorer, Chrome, and Firefox browsers.
• User-friendly interface for managing scientific literature, patents, and research findings electronically.
• Cloud-based deployment reduces the need for on-site infrastructure.

Support and Global Availability

• Used by clients across the USA, UK, Europe, Korea, Japan, China, and India.
• Includes dedicated support for implementation, training, and ongoing operational assistance.
• Transparent pricing model aimed at providing a cost-effective solution for literature management workflows.

Clinevo Literature Automation is deployed as a cloud solution and is built to meet regulatory standards including 21 CFR Part 11, Annex 11, GxP, and GDPR. It integrates with major PV databases and is designed to support the full literature management lifecycle from automated retrieval through compliance documentation and reporting.