QPPV

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 minimization 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.”