Bibliovigilance / Pharmacovigilance
Automated Scientific Literature Search Platform
Bibliovigilance Core Features
- National and global searches
- Create and group your searches once, run on demand
- Search within scope (national literature, Pubmed and PRAC Recommendations)
- Schedule automatic searches and be notified of new results
- Search only for the previous week's articles
- Build a library of your company's articles of Interest
- Centralise all your pharmacovigilance needs in one location
- Compliant with EMA and FDA guidelines
Scientific and medical literature stands as an essential foundation for tracking safety profiles and managing the risk-benefit balance of active medicinal products. It is key for identifying newly emerging safety issues and critical safety signals early.
To meet regulatory requirements, marketing authorization holders must systematically review reference databases at least once a week. This follows EMA's Good Pharmacovigilance Practices guidelines (GVP Module VI).
Bibliovigilance streamlines your routine literature reviews within a single automated workspace.
By connecting national and international resources into one secure platform, it removes manual multi-source cross-referencing and cuts structural operational overhead for safety teams across Europe.
Explore full platform capabilities and independent case studies directly at the Bibliovigilance Product Portal.
Platform Highlights & Deep-Dive Details
Full monitoring transparency with immediate access to active index logs.
Safety teams get full disclosure over indexed sources, with complete on-demand views of every local and global scientific publication tracked within the Bibliovigilance master index.
Localized European Indexing
The platform maintains a curated database that indexes dozens of the most critical national medical and scientific publications across key European countries, alongside PRAC signal recommendations.
Centralized Data Aggregation
By pairing local medical journals with global source repositories, the system ensures local country reporting stays fully aligned with overarching safety monitoring workflows.
Configure medical product search terms once, then automate your pipeline.
The platform eliminates repetitive manual queries by letting users save and group complex drug screening matrices into automated tracking templates.
On-Demand vs Automated Execution
Schedules can be set to trigger screening updates automatically at designated intervals, or run instantly with a single click before urgent internal review cycles.
Delta Filtering Controls
Refine your search parameters to isolate new articles published since a specific term was last run. This simplifies screening steps by keeping teams focused on newly indexed content.
Comprehensive query histories preserved in secure team workspaces.
All executed search processes are permanently cataloged inside a secure, authorized personal workspace area to ensure search strings and validation steps remain fully traceable for future regulatory audits.
Articles of Interest Library
Users can flag target publications to build a structured, company-wide internal library of relevant safety findings. This makes it easy to quickly share, reference, and retrieve documentation when assessing emerging risks or processing safety signals.