Expert QPPV & LPPV
for a Compliant Global PV System
for a Compliant Global PV System
A Qualified Person for Pharmacovigilance (QPPV) plays a critical role in ensuring that a Marketing Authorisation Holder (MAH) maintains a compliant and effective global pharmacovigilance (PV) system. The QPPV is responsible for overseeing PV operations, regulatory compliance, and safety reporting across all territories. In addition, Local Person for Pharmacovigilance (LPPV) are required in many countries to ensure compliance with local regulations and to support a fully integrated global PV framework. Our expert services help you establish and manage both QPPV oversight and LPPV networks, ensuring seamless compliance with global and regional PV requirements.
Our QPPV and LPPV Services leads
Seema Jaitly
Pharmacovigilance Physician
Shelley Forword
PV Consultant, QPPV/LPPV Management & PV Systems
Our QPPV & LPPV Services
Local PV Services & Compliance
- Local PV Services & Regulatory Support – Country-specific compliance solutions.
- LPPVs – Covering the EEA, UK, Switzerland, and additional regions.
QPPV Office & Global Oversight
- EU QPPV & Deputy QPPV – Ensuring compliance with EU pharmacovigilance requirements.
- UK QPPV & Deputy, plus National Contact Person (NCP) – Meeting UK-specific PV obligations.
- Local QPPVs – Available in LATAM, MENA, CIS, and other global regions.
- QPPV Handover Support – Smooth transition of QPPV responsibilities for business continuity.
Safety & Regulatory Operations
- ICSR Follow-up & Local Literature Review – Ensuring timely case processing and reporting.
- Management of Local Regulatory Portals – Including EudraVigilance (EV), XEVMPD, MHRA, ELViS, and others.
- Pharmacovigilance System Master File (PSMF) Management – Ensuring compliance with global PV regulations.
