Pharmacovigilance

Pharmacovigilance Audits and Training

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

Inspection-Ready Teams and Systems

Pharmacovigilance systems must be audited regularly, and staff involved in pharmacovigilance must be trained for their tasks, as described in GVP Modules IV and I.

URAS PV supports you with audits of your PV system and partners, preparation for regulatory inspections, and training programmes tailored to each team's role.

Our services include:

  • Internal audits of the pharmacovigilance system
  • Audits of PV service providers and partners
  • Inspection readiness assessments and mock inspections
  • Corrective and preventive action (CAPA) follow-up
  • Role-based pharmacovigilance training
  • Training records and documentation

How We Work

01

Plan

Audit scope and training needs are defined based on risk.

02

Perform

Audits and training sessions are carried out and documented.

03

Improve

Findings are followed up through CAPAs until closure.

Other Pharmacovigilance Services

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

Entrust your pharmacovigilance responsibilities to us.

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

Request a Free Assessment