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

GRP Presentations on PV

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