Pharmacovigilance

Global PSMF Writing and Management

Writing your global Pharmacovigilance System Master File, keeping it current and inspection-ready at all times.

An Accurate Description of Your PV System

The Pharmacovigilance System Master File (PSMF) describes the pharmacovigilance system used by the marketing authorisation holder for its authorised products. Its content and maintenance are described in GVP Module II.

URAS PV writes the global PSMF and its annexes, prepares national or local versions where local legislation requires them, keeps the file up to date as your system changes, and makes sure it can be provided to competent authorities whenever requested.

Our services include:

  • Writing of a global PSMF and its annexes
  • National or local PSMF documents where required by local legislation
  • Gap analysis of an existing PSMF
  • Regular updates and change control with a logbook
  • Maintenance of PSMF annexes, including product lists and contracts
  • Support during inspections and authority requests

How We Work

01

Assessment

We review your PV system, procedures and existing documentation.

02

Writing

We write or restructure the global PSMF and its annexes.

03

Maintenance

We record changes and keep the PSMF current and inspection-ready.

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

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

Entrust your pharmacovigilance responsibilities to us.

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

Request a Free Assessment