Access to all data around clinical trial regulations, ICSR reporting (domestic and foreign cases), and DSURs.

All the safety information you need to plan and operate a clinical study.

Pricing is per user.

Access all country data.

Includes regulations, clinical and post-marketing reporting, managed access programs, aggregate reports, QPPV, PSMF, Signal Management, and RMP.

Pricing is per user.

Full access to the database.

Create a custom GxP repository to track and maintain company or product-specific pharmacovigilance requirements.

Unlimited users & countries.