According to Eurasian Economic Union (EAEU) requirements all pharmaceutical companies that register medical products on the market must appoint a Qualified Person For Pharmacovigilance (QPPV). This is the person who interacts with regulatory authorities and is responsible for the provision and operation of the company’s pharmacovigilance system.

With a strong experience in pharmacovigilance, X7 Research offers a full range of QPPV services in the EAEU that enable you to meet the pharmacovigilance requirements of the market.

routine PV activities

PV sistem update

PSUR/DSUR/RMP preparation and submission

X7 Research provide PV services since 2010. Our clients are local companies as well as Big Pharma.