Pharmacovigilance

Validated Safety Database

A single platform for ICSR management, coding and regulatory submissions.

Your Safety Data in One Place

A pharmacovigilance safety database stores individual cases, supports MedDRA coding and generates the electronic reports and listings required by authorities.

URAS PV's validated safety database unifies ICSR management, coding and regulatory submissions on a single platform, so your safety data is consistent, traceable and ready for analysis.

Our services include:

  • Case entry and workflow management
  • MedDRA coding
  • Electronic ICSR generation and submission
  • Line listings and data outputs for periodic reports
  • Audit trail and access control
  • Support for signal detection and safety analyses

How We Work

01

Set-Up

Your products and reporting rules are configured in the database.

02

Operation

Cases are processed with full traceability and controlled access.

03

Reporting

Submissions, listings and outputs are generated from one source.

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

Audit & Training

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

Audit and training details

Entrust your pharmacovigilance responsibilities to us.

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

Request a Free Assessment