Date of Publication: 02-Feb-2026
INTELLIGENCE OVERVIEW
Agency: EMA
The European Medicines Agency (EMA) has released updated guidance on the registration process for users accessing the Union Product Database (UPD). This document explains the prerequisites for UI and API access, including EMA Account Management (EAM), Organisation Management Service (OMS) registration, and role-based approvals for competent authorities, pharmaceutical industry, and public users.
The guidance aims to support seamless onboarding and secure access to UPD for regulatory submissions and data exchange across the EU.
KEYWORDS: Regulatory Compliance, Union Product Database (UPD), Organisation Management Service (OMS)
REFERENCE: https://www.ema.europa.eu/en/documents/other/upd-registration-guide-ui-api-users_en.pdf , https://www.ema.europa.eu/en/news-events/whats-new