EU QPPV Services
Qualified Person for Pharmacovigilance (QPPV) services for the European Union.
About Us
One group. Four specialised divisions.
Bpharma
Site Management Organisation
Bpharma
Clinical Operations
Bpharma
Regulatory strategy, licensing & lifecycle
Bpharma
Pharmacovigilance

Local safety officers, system set-up, literature screening, regulatory intelligence and QPPV services.
You stay focused on your products and patients. We take care of the local PV complexity.
Bpharma builds compliant local pharmacovigilance systems that connect your global PV organisation with country-specific requirements.
Dedicated Qualified Person for Pharmacovigilance (QPPV) services across the Eurasian Economic Union (EAEU), supporting Marketing Authorisation Holders (MAHs) in maintaining a compliant, effective and inspection-ready pharmacovigilance system.
Bpharma combines technology-enabled literature screening with pharmacovigilance expertise to identify, assess and manage safety information from global scientific publications, supporting regulatory compliance and patient safety.
Pharmacovigilance regulations are constantly evolving. Bpharma helps pharmaceutical and biotechnology companies stay informed, understand the impact of regulatory changes and maintain compliance across their markets.
Qualified Person for Pharmacovigilance (QPPV) services for the European Union.

QPPV: Qualified Person for Pharmacovigilance · EAEU: Eurasian Economic Union · SDEA: Safety Data Exchange Agreement · PSMF: Pharmacovigilance System Master File