ProRelix Research has a 20-year collective experience of their experts and history of handling complex and sensitive interactions in the life sciences industry. From basic medical inquiries to complex adverse event intake, case processing and aggregate reporting, ProRelixResearch provides an end-to-end solution for all of your Pharmacovigilance needs including product safety, medical information and regulatory compliance – all leveraging our global multi-channel, multi-lingual contact centers. Whether you’re a large pharmaceutical manufacturer, optimizing drug safety across your entire marketed portfolio, or a smaller biotech with a single emerging compound, ProRelixResearch is the perfect addition to your safety strategy. At ProRelix Lifesciences we offer end to end Pharmacovigilance services including medical contact center, Individual case safety reports, medical reviews, SAE narratives, ADR analysis, regulatory compilation and submission.

Medicine and ergonomics - studies and research
  • Quality assurance
  • safety writing
  • pharmacovigilance
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