Regulatory & Compliance GxP

MDR

MDR is the validated data backbone for EU MDR — turning scattered device data into compliant submissions and feeds.

1.2M+

Device records published

submitted to health authorities to date

12+

Source systems consolidated

UDI, quality and EUDAMED inputs unified

Downstream feeds served

regulatory and quality systems fed

Figures are illustrative placeholders for this preview — live metrics integration from each solution's source is planned.

Watch the overview

A 2.2 min walkthrough of what MDR does and the value it delivers.

MDR is the validated data backbone for EU MDR — turning scat

Overview

MDR (RDB MDR Data Management) is a centralized, GxP-validated data platform that consolidates device data from many MedTech source systems and prepares it for the EU Medical Device Regulation program. It ingests, curates, standardizes and publishes Unique Device Identification, commercial quality and EUDAMED actor data — then delivers it as governed delta and bulk feeds to regulatory and quality systems such as ReedTech for UDI publication, Enterprise Complaints Management and Technical Documentation. If your franchise sells devices in the EU, MDR is the trusted source that keeps your device records accurate, auditable, and submitted to health authorities.

What it does

Ingest, curate and standardize device data from many source systems
Publish UDI records to health authorities via ReedTech
Submit EUDAMED actor registration data
Consolidate commercial quality feeds into one trusted source
Deliver governed delta and bulk feeds to downstream consumers
Run a GxP-validated, audit-ready data pipeline

Getting access

For access to MDR, or for any data or integration request, contact the listed application owner. The team will assess your requirements and recommend the best approach for your use case.

Overview text is a draft for this preview, pending review by the application owner.