Pharmacovigilance

Pharmacovigilance Services

End-to-end pharmacovigilance services, from QPPV and PSMF to case processing, signal management and audits, for global and local markets.

End-to-End Pharmacovigilance Services

From pre-authorisation to lifecycle management, we stand by you in every phase.

Global & Local Pharmacovigilance

We build global PV systems fully compliant with international standards (ICH, GVP) and act as local LPPV representatives in 15+ countries.

Global and local pharmacovigilance details

QPPV Outsourcing

We assume marketing authorisation holders' legal obligations with our EU QPPV, UK QPPV, and country-based qualified person (LPPV) services.

QPPV outsourcing details

PSMF Management

Full-scope support for creating, maintaining, and keeping the Pharmacovigilance System Master File (PSMF) inspection-ready at all times.

PSMF writing and management details

SOP Writing

Writing and review of pharmacovigilance SOPs and working instructions aligned with GVP and local requirements.

SOP writing details

ICSR Processing

Collection, assessment, coding (MedDRA), and electronic submission of Individual Case Safety Reports (ICSR) to systems such as EudraVigilance and FDA FAERS.

ICSR processing details

Signal Management & Risk Assessment

Proactive signal detection, benefit-risk analysis, and the preparation of periodic safety reports (PBRER / DSUR).

Signal management details

Literature Monitoring

Continuous monitoring of global and local literature (PubMed + local journals), case identification, and reporting.

Literature monitoring details

Safety Database

Our validated safety database unifies ICSR management, coding, and regulatory submissions on a single platform.

Safety database details

Audit & Training

PV audit preparation, internal audit services, and regulatory training programmes for your teams.

Audit and training details
CIS & Türkiye

Pharmacovigilance in the CIS, EAEU and Türkiye

Our expertise includes Local QPPV and EAEU QPPV services, Individual Case Safety Report (ICSR) management, local literature monitoring, pharmacovigilance system documentation, and regulatory support.

Pharmacovigilance across the CIS and Türkiye

Countries Covered by URAS PV

  • Azerbaijan
  • Georgia
  • Kazakhstan
  • Kyrgyzstan
  • Moldova
  • Türkiye
  • Ukraine
  • Uzbekistan

Entrust your pharmacovigilance responsibilities to us.

Talk to our team and let us design a tailored solution for you.

Request a Free Assessment