BlueReg can also provide you with a EU-QPPV (European Qualified Person Responsible for Pharmacovigilance), French QPPV, or deputy of when needed (e.g.: illness, leave). You can have confidence in our consultants who keep their knowledge and training up to date.


The QPPV is responsible for:


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


“All these missions are carried out according to the requirements and modalities of Good Vigilance Practices and local standards.”



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