From pets to livestock, we bring AI-driven surveillance to every corner of veterinary pharmacovigilance.
The regulatory landscape for veterinary medicines is evolving fast — from EU Regulation 2019/6 to FDA CVM requirements and national frameworks. Biologit supports marketing authorisation holders (MAHs), sponsors and applicants in meeting these obligations with confidence.
Think of us as your virtual safety surveillance partner — helping maintain your systems and processes for animal, human, and environmental safety.
Coverage of journals, regional publications, and offline sources to detect emerging safety signals.
Expert development and maintenance of SOPs and compliance documentation to ensure regulatory readiness.
Qualified oversight and regulatory representation for veterinary medicinal products (VMPs).
Deployment support, team training, and long-term pharmacovigilance strategy.
Our GxP-validated, fully traceable platform combines a unified scientific database, flexible workflows, and AI-powered productivity features. It’s built to help veterinary safety teams manage large-scale literature workloads efficiently, accurately, and in full compliance.
Biologit delivers efficiency, compliance, and control — all in one place
