Qualified Person for Pharmacovigilance (QPPV)

A Qualified Person for Pharmacovigilance (QPPV) plays a pivotal role in maintaining drug safety throughout the lifecycle of pharmaceutical products. Acting as the central figure in pharmacovigilance operations, the QPPV is responsible for overseeing adverse drug reaction (ADR) reporting, ensuring regulatory compliance, and upholding patient safety.

The QPPV serves as a 24/7 point of contact for regulatory authorities and is supported by a designated backup QPPV during absences. Together, they ensure seamless operation of the pharmacovigilance system, continuous risk-benefit monitoring, and the safe use of authorized products in the market.

At Scansio, we offer specialized QPPV services to support companies in meeting global pharmacovigilance obligations with confidence.

Our QPPV Services Include:

• End-to-End Oversight of Pharmacovigilance Activities
• Acting as Primary Liaison with Health Authorities
• Monitoring and Managing Risk Signals
• Timely Adverse Event Reporting
• Ensuring PV System Compliance with Current Regulations
• Supporting Pharmacovigilance Inspections and Audits
• Providing Comprehensive PV Training

Scansio maintains a global network of experienced QPPVs with deep regulatory insight and hands-on expertise in managing robust pharmacovigilance systems across diverse markets.