ISO IDMP Compliant

Regulatory compliance,
simplified.

VeMPS is the all-in-one Veterinary Medicinal Products System built for pharmaceutical companies. Manage licences, track renewals, and stay IDMP-compliant — all from one intelligent dashboard.

Start Free Trial Request a Demo
ISO 11615 / 11616 / 11238 / 11239
360° Licence Lifecycle Visibility
Multi Jurisdiction & Agency Support
VeMPS Dashboard
■ Dashboard
■ Authorisations
■ Products
■ Substances
■ Organisations
■ Documents
Welcome back, Sarah
Due ≤ 30 days
3
Renewals urgent
Due ≤ 90 days
11
Renewals upcoming
Active
84
Authorisations
Upcoming Renewals
ProductCountryExpiresStatus
Cardivex 5mgDE2026-06-18 Urgent
Nephrex 10mgFR2026-07-04 Soon
Lumivax 50mgGB2026-08-21 On Track
The Challenge

Regulatory complexity costs time — and compliance.

📋

Fragmented data

Licence data spread across spreadsheets, email threads, and shared drives creates dangerous blind spots.

⏰

Missed deadlines

Renewal dates slip through the cracks when there's no centralised, proactive alerting system.

🌍

Multi-jurisdiction complexity

Keeping track of requirements from EMA, MHRA, and national agencies simultaneously is overwhelming.

📄

Audit risk

Inconsistent records and missing document trails expose organisations to serious regulatory risk.

VeMPS solves all of this — in one place, with one system.
Features

Everything your regulatory team needs

Built specifically for pharmaceutical regulatory affairs teams, VeMPS brings clarity to the most complex licensing environments.

🛡️

Proactive Renewal Alerts

Colour-coded urgency indicators flag licences expiring within 30 or 90 days. Your team always knows what needs attention — before it becomes a problem.

  • Red Expires within 30 days — act now
  • Amber Expires within 90 days — plan ahead
  • Green On track — nothing to worry about
📂

Full Licence Lifecycle

Track every authorisation from initial grant through variations, renewals, suspensions, and withdrawals. Complete history at your fingertips.

🔗

IDMP Hierarchy

View the complete IDMP data hierarchy for every licence — Medicinal Product, Pharmaceutical Product, Substance, and Organisation — all linked.

📑

Document Management

Upload and version SmPCs, PILs, Assessment Reports, and all regulatory documents. Link them directly to licences and events.

🔍

Powerful Search

Find any product, substance, or organisation instantly. Filter licences by status, country, procedure type, or authorisation type.

📅

Regulatory Event Log

Record Type IA, IB, and II variations with submission, approval, and implementation dates. A permanent, auditable trail.

🌐

Multi-Jurisdiction

Manage licences across all EU member states, GB, and beyond. Track centralised, MRP, DCP, and national procedures side by side.

🔒

Enterprise Security

JWT authentication, role-managed user accounts, session controls, and route guards protect your sensitive regulatory data.

IDMP Standards

Built on ISO IDMP from the ground up

VeMPS is not retrofitted for IDMP — it is architected around it. Every data model aligns with the ISO standards that regulators require.

ISO 11615
Medicinal Products
MPID — unique identifier for each authorised medicinal product, with therapeutic area, ATC code, and legal status.
ISO 11616
Pharmaceutical Products
PhPID — dose form, route of administration, and unit of presentation mapped per standard.
ISO 11238
Substances
UNII / GSRS registry support with INN and CAS number for unambiguous substance identification.
ISO 11239
Organisations
LOC_ID location identifiers for MAHs and manufacturers — fully traceable across jurisdictions.
How It Works

Up and running in three steps

01

Connect your data

Point VeMPS at your SQL Server database. Run our migrations or import from an existing schema. No manual re-entry required.

→
02

Populate your portfolio

Register your medicinal products, substances, organisations, and authorisations. The built-in REST API supports bulk ingestion from existing systems.

→
03

Manage with confidence

Your team logs in, sees the dashboard, and immediately knows what needs action. Renewals tracked, documents linked, events logged.

Technology

Enterprise-grade, modern stack

VeMPS is built on technology your IT team already trusts — no exotic dependencies, no proprietary lock-in.

ASP.NET Core Web API backend — high-performance, cross-platform, enterprise-ready.
Angular 17 standalone components — fast, type-safe, single-page application frontend.
Entity Framework Core on SQL Server — robust data persistence with full migration support.
Stateless JWT authentication — secure, scalable, integrates with enterprise identity providers.
Full OpenAPI/Swagger documentation included — third-party integrations made easy.
End-to-end TypeScript type safety from API contracts to UI components.
Get Started

Ready to take control of your regulatory portfolio?

Request a personalised demo and see VeMPS working with your data in under 30 minutes.

Don't want to wait? Start your free trial →