PrimeVigilance, an Ergomed company, was set up by former Pharmacovigilance Regulators in 2008. We have grown to become the leading Pharmacovigilance specialist company, delivering global solutions for both clinical safety and post-marketing pharmacovigilance, as well as medical information from our offices. Having successfully delivered Pharmacovigilance (PV) and Medical Information (MI) services for over 14 years, our experience enables us to offer a comprehensive, top quality, cost-effective, and innovative safety solution. Our flexible approach, tailor-made to work with clients, allows us to deliver the services that meet your clinical and post-marketing needs.
From its operational hubs based in Europe, the USA, and Japan. PrimeVigilance manages a global Pharmacovigilance system with a choice of leading drug safety databases, stretching to more than 100 countries.
• 900+ highly qualified professionals
• Global leader in QPPV services
• 24/7 multilingual call center
• Choice of leading drug safety databases
• Robotic Process Automation (RPA) expertise
• Access to regulatory experts and key opinion leaders

GLOBAL LIFE CYCLE MANAGEMENT SERVICES
• PHARMACOVIGILANCE 
• PHARMACOEPIDEMIOLOGY & BENEFIT-RISK MANAGEMENT
• AUDIT & INSPECTION
• QUALITY MANAGEMENT
• REGULATORY SCIENCE 

Pharmaceutical

PrimeVigilance

PrimeVigilance's headquarters in Guildford, United Kingdom

Dave Selkirk

Adebunmi Urakpo

The Pharmacovigilance Specialists team at PrimeVigilance is dedicated to ensuring the safety and efficacy of pharmaceutical products throughout their life cycle. This team conducts comprehensive monitoring and analysis of drug safety data, manages adverse event reports, and ensures compliance with global regulatory standards. By leveraging their extensive expertise, they provide critical insights that inform benefit-risk assessments and enhance patient safety across a wide range of therapeutic areas.

Pharmacovigilance Specialists

The Medical Writing and Communication team at PrimeVigilance is responsible for creating and managing high-quality scientific documentation related to pharmacovigilance and medical information. This includes writing clinical study reports, safety narratives, and regulatory submissions, while ensuring compliance with industry standards and regulatory requirements. The team also facilitates clear communication of complex medical data to stakeholders, supporting the company’s commitment to delivering innovative safety solutions and comprehensive medical information services.

Medical Writing and Communication

The Regulatory Affairs and Quality Management team at PrimeVigilance ensures compliance with global regulations and quality standards in pharmacovigilance and medical information services. This team works collaboratively to oversee regulatory submissions, manage audits and inspections, and implement quality management systems, ensuring that processes meet both client and regulatory expectations while maintaining the highest level of safety and efficacy for pharmaceutical products.

Regulatory Affairs and Quality Management

The Leadership Team at PrimeVigilance is responsible for setting the strategic direction of the company, ensuring operational excellence, and fostering innovation in pharmacovigilance and medical information services. Comprising key executives including the President and Chief Financial Officer, this team collaborates to drive growth, manage resources, and uphold the company's commitment to delivering high-quality, client-focused safety solutions on a global scale. Their leadership ensures that PrimeVigilance remains at the forefront of the industry, navigating regulatory landscapes and aligning with best practices.

PrimeVigilance

Org chart

Teams

Pharmacovigilance Specialists

Medical Writing and Communication

Regulatory Affairs and Quality Management

Leadership Team

Offices

PrimeVigilance

Org chart

Teams

Pharmacovigilance Specialists

Medical Writing and Communication

Regulatory Affairs and Quality Management

Leadership Team

Offices

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