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Veterinary Pharmacovigilance

Meeting the Challenges in Veterinary Pharmacovigilance Regulations

The Veterinary Medicinal Products (VMP) environment is growing and increasing its regulatory requirements for pharmacovigilance. Global requirements for safety surveillance and pharmacovigilance include the (EU) 2019/6, Commission Implementing Regulation (EU) 2021/1281, FDA CVM regulations, VMD UK: The Veterinary Medicines Regulations 2013 SI 2033, and other global regulations.

Pharmacovigilance Regulations

Your Partner in Veterinary Pharmacovigilance

As your global partner, our veterinary experts can assist sponsors, marketing authorization holders (MAHs), and applicants with their veterinary pharmacovigilance needs. Biologit can act as a virtual safety surveillance department for veterinary companies, supporting and maintaining their safety systems with a focus on animal, human and environmental safety, research and development, regulatory approval and post market surveillance.

Pharmacovigilance Systems for Veterinary Products

Scientific and Medical Literature Monitoring

Quality Systems for Veterinary Medicinal Products

Veterinary QPPV (Qualified Person for Pharmacovigilance)

Project Planning and Training

Veterinary Pharmacovigilance
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Literature Monitoring for Veterinary Pharmacovigilance

Monitoring the scientific literature for adverse events is a critical component for active safety surveillance of post-market veterinary products and regulatory submissions.

The biologit's MLM-AI platform is a validated and compliant SaaS solution for veterinary companies, providing a flexible workflow, unified scientific database, and unique AI productivity to help ensure your products are compliant and all data is audit ready.

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