Pharmacovigilance

Overview

Pharmacovigilance has been defined by the World Health Organization (WHO) as the science and activities related to the detection, assessment, understanding and prevention of adverse effects or any other medicine-related problem.
Global Regulatory Partners Inc. (GRP) provides end-to-end global pharmacovigilance services for Pharma, Medical Device, Nutraceutical and Cosmetic companies worldwide in order to optimize the products’ benefit-risk profile to improve safety and achieve better patient outcomes. GRP’s Pharmacovigilance team have long standing industry experience and consistently deliver, high quality and compliant Pharmacovigilance services.

GRP Pharmacovigilance Services

  • Receipt, review and coding of adverse events
  • Safety reports writing
  • Safety reporting to different health authorities
  • Good Vigilance Practice (GVP)
  • Product safety profile building
  • Product safety profile continuous update
  • Post-Marketing Surveillance (PMS) studies
  • Safety annual reports
  • Medical literature screening
  • Health authority PV database monitoring
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