Animal Health
Medical Information and Pharmacovigilance Services
Comprehensive solutions for animal heath regulatory needs
Animal Health Experience & Capabilities
24/7/365
Fully integrated, decentralized 24/7/365 contact center.
24/7/365
Fully integrated, decentralized 24/7/365 contact center.
Read LessFDA, NASC, EPA, USDA, PMRA
Experience helping clients maintain compliance with regulatory agencies.
FDA, NASC, EPA, USDA, PMRA
Experience helping clients maintain compliance with regulatory agencies.
Read LessHighly Qualified Experts
Our team includes experienced veterinarians, pharmacists, veterinary technicians, and other healthcare professionals.
Highly Qualified Experts
Our team includes experienced veterinarians, pharmacists, veterinary technicians, and other healthcare professionals.
Read LessProPharma’s Animal Health Expertise
ProPharma provides comprehensive Animal Health Medical Information (MI) and Pharmacovigilance (PV) support services, including expertise with the multiple regulatory environments that varied species and active ingredients require. ProPharma service comprises a fully integrated 24/7/365 contact center to deliver current and accurate information and improve patient health and safety as well as a team of PV experts to ensure the highest levels of compliance. ProPharma’s Animal Health team includes experienced veterinarians, pharmacists, veterinary technicians, and other healthcare professionals. This enables us to respond to medical inquiries in a manner that is not only consistent with product labeling and regulatory guidance, but also recognizes the connection between animals and people and the importance of communication between interdisciplinary healthcare professionals.
With a decentralized 24/7/365 contact center, ProPharma’s team of experts provides a customized solution to fit the medical information and pharmacovigilance needs of companies of all sizes. Whether you need to augment your internal team or need to completely outsource the Animal Health MI or PV functions globally, ProPharma has the right solution for your specific needs.
Animal Health & Toxicology Medical Information Contact Center
We offer comprehensive support around the clock. Our global 24/7/365 contact center provides crucial services, including Adverse Event (AE) intake and follow-up, Product Complaint (PC) management, and Medical Information inquiry fulfillment with escalation protocols. Our qualified MI/TOX specialists utilize market‐leading technologies to help clients deliver current and accurate information and improve patient health and safety.
We specialize in handling accidental exposure triage with thorough toxicology assessments and follow-up. Additionally, our team is adept at crisis detection and executing client emergency bullhorn actions, ensuring rapid and effective responses to urgent situations.
Our Animal Health team includes expertise with the multiple regulatory environments that varied species and active ingredients require, ensuring the highest levels of compliance. The team includes experienced veterinarians, pharmacists, veterinary technicians, and other healthcare professionals.
Animal Health Medical Writing and Content Management
Our team excels at medical writing and content management for your animal health products, leveraging our extensive expertise across various therapeutic areas and academic settings. We offer a range of services including standard document creation, custom response and content management, and response document maintenance. Additionally, our translation and localization services ensure that your critical documentation is accessible and relevant to diverse audiences.
Animal Health Pharmacovigilance Services
We ensure the highest standards of safety and compliance. Our services include comprehensive Adverse Drug Experience (ADE) assessment and processing, preparation and review of FDA Center for Veterinary Medicine (FDA CVM) ADE reports, and robust signal detection and management. We also offer seamless integration of regulatory services for non-FDA products, including but not limited to NASC, EPA/FIFRA, USDA, and Health Canada/PMRA, addressing all your pharmacovigilance needs.
Contact Us for Expert Animal Health Support
We are dedicated to enhancing the health and well-being of animals through our comprehensive Medical Information and Pharmacovigilance services. Whether you need reliable medical information, safety monitoring, or compliance support, our team of experts is here to help.
Meet Our Animal Health Experts
-
Dane Goede
Traditional Call Center Manager
View Bio
-
Karen Gjevre
Medical Information Supervisor, Traditional Call Center
View Bio
Dane Goede
Karen Gjevre
News & Insights
October 21, 2026
From Defensible to Predictive: How High-Functioning MLR Teams Are Evolving Their...
Recent FDA enforcement activity is changing how MLR teams assess promotional risk. Learn why organizations are moving from defensible claims to predictive, enforcement-informed risk assessment.
October 19, 2026
AI-Readiness 101: AI Success Starts with Understanding Your Data
Unlock AI success by understanding your data. Learn the foundations of AI readiness and how to build trust in your data for reliable insights.
July 8, 2026
ProPharma Advances Technology Enablement Strategy with AI-Assisted Capability fo...
ProPharma unveils an AI-assisted capability to enhance ANDA submission development, improving efficiency and maintaining regulatory excellence for clients.
June 18, 2026
ProPharma Welcomes Kevin van Dooren to Strengthen Integrated EU Regulatory and H...
ProPharma welcomes Kevin van Dooren as Vice President, HEOR and Market Access, strengthening integrated EU regulatory, HTA, reimbursement, and market access capabilities for life sciences companies.
January 31, 2025
ProPharma Recognized for AI Excellence at ECCCSA
ProPharma wins Silver at ECCCSA for AI innovation in Medical Information, enhancing efficiency and quality in delivering accurate medical information.
October 9, 2024
ProPharma Receives 2024 CPHI Regulatory and Compliance Award
ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.
October 20, 2026
Accelerating Clinical Trial Activation Across Latin America
Launching clinical trials across multiple countries requires navigating varying regulatory requirements, site contracts, translations, import/export processes, and site engagement activities, all...
September 18, 2026
Flexible Resourcing Without Limits: Scaling Capabilities Across the Development ...
Development complexity doesn’t increase in a straight line. As programs progress from discovery through Phase III, submission, and post-approval, demands for medical writing, biometrics, clinical...
August 3, 2026
Achieving Continuous Audit Readiness Across a Global Medical Information Program
Maintaining continuous audit readiness across a global Medical Information operation requires more than periodic audit preparation. Organizations operating across multiple countries and affiliates...
December 2, 2026
Beyond the Buzz: Leveraging Community Management to Enhance Medical Information
Patients, caregivers, and healthcare professionals are increasingly turning to digital channels to seek information, share experiences, and discuss treatments. Join this webinar to explore how...
November 12, 2026
Empowering Sites, Engaging Patients: Strategies to Improve Clinical Trial Performance
Sites are being asked to do more than ever before while balancing increasing trial complexity, patient expectations, and operational demands. Join this webinar to explore how flexible, integrated...
News & Insights
September 18, 2026
Flexible Resourcing Without Limits: Scaling Capabilities Across the Development ...
Development complexity doesn’t increase in a straight line. As programs progress from discovery through Phase III, submission, and post-approval, demands for medical writing, biometrics, clinical...
August 3, 2026
Achieving Continuous Audit Readiness Across a Global Medical Information Program
Maintaining continuous audit readiness across a global Medical Information operation requires more than periodic audit preparation. Organizations operating across multiple countries and affiliates...
November 12, 2026
Empowering Sites, Engaging Patients: Strategies to Improve Clinical Trial Performance
Sites are being asked to do more than ever before while balancing increasing trial complexity, patient expectations, and operational demands. Join this webinar to explore how flexible, integrated...