Pharmacovigilance Solutions

Pharmacovigilance Solutions

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Whether the path ahead includes a first-in-human investigative trial or global product approval, we’re here to help. From clinical development through post-marketing surveillance, your team can rely on our industry-leading PV specialists providing a full suite of services to ensure your PV system fulfills regional and global regulations, and continuously monitors the safety of your products. ProPharma offers stand-alone contracts utilizing our myriad PV services or integration with global Clinical Research Services, Medical Information, or Regulatory services.
ProPharma71For the past 20+ years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

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