Qualified Person Responsible for Pharmacovigilance (QPPV)

BlueReg can provide you with a EU-QPPV (European Qualified Person Responsible for Pharmacovigilance), French QPPV and/or deputy on a permanent basis or when required (e.g.: illness, etc). You can have confidence in our qualified consultants who ensure their knowledge and training is fully maintained.


The QPPV is responsible for:


  • Establishing and maintaining a pharmacovigilance system
  • Preparing pharmacovigilance reports
  • Setting-up of risk minimisation studies
  • Answering requests from Health Authorities
  • Providing Health Authorities with any other information relevant to product safety


“All these activities are carried out in full compliance with Good Vigilance Practices and local standards.”

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