Enhancing Animal Health Compliance With Comprehensive MI And PV Services
By Valerie Huh, Director, Global Innovation and Implementation

In the veterinary industry, regulatory compliance is vital for ensuring the safety and efficacy of animal health products, particularly given their impact on public health. The FDA’s Center for Veterinary Medicine (CVM), along with international bodies like the EMA and USDA, enforces stringent requirements for pharmaceuticals, vaccines, and related products. To navigate this complex landscape, veterinary companies must implement robust Medical Information (MI) and Pharmacovigilance (PV) practices.
MI services handle inquiries, adverse event (AE) reporting, product complaints, and crisis management, ensuring accurate, consistent information aligns with regulatory standards. PV services focus on tracking and reporting Adverse Drug Experiences (ADEs), conducting safety signal detection, and preparing regulatory submissions, particularly for the FDA CVM. These practices help prevent regulatory actions such as fines or product recalls. ProPharma offers comprehensive MI and PV support, leveraging decades of expertise to help veterinary companies meet regulatory requirements, maintain product safety, and build stakeholder trust, ensuring the highest industry standards.
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