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Our team of qualified experts combined with integrated technology ensure your product meets the highest levels of compliance with both regional and global regulations.

We have the flexibility and capability to scale our services for small clients with a single clinical trial, through to global multinationals with marketed products that create high case volumes requiring 24/7/365 support. Our PV services are available on a standalone basis or can be integrated with global Medical Information and Regulatory services.

The ProPharma Group Advantage

QPPV and LPPV Services

Fully qualified specialists with deep experience in pharmaceuticals, regulatory, and academia

Single-Source Provider

Global, independent, single-source provider of RA, Life Science Consulting, PV, and MI services

24/7/365 Multilingual Services

“Follow the sun” capabilities and native-speaking specialists in more than 35 languages

A Global Team of Trusted Experts

Our PV team consists of experienced healthcare professionals such as PharmD, Nurses, and Medical Doctors and works as your collaborative pharmacovigilance partner in support of our mission to improve patient health and safety. Whether you need standalone services or integrated global pharmacovigilance, medical information and regulatory services, ProPharma Group can support your specific needs.

Contact Us

Need Help Managing Your Drug Safety Requirements?

Contact us to learn how our clinical and postmarketing PV services can support your needs on a standalone basis or integrated with global Medical Information and Regulatory services.

Interested in gaining an industry edge? Let us help you stay current.

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