---
title: "EU Readiness Assessments | QbD Group"
description: "Free EU readiness assessments for medical devices, pharmaceuticals, and cardiology clinical trials. Identify compliance gaps in 10–15 minutes."
url: https://qbdgroup.com/en/eu-readiness
type: "Page"
language: en
publisher: "QbD Group"
citation: "QbD Group, \"EU Readiness Assessments | QbD Group\", https://qbdgroup.com/en/eu-readiness"
---

Free Compliance Check

# Is Your Organization EU-Ready?

Choose the assessment that matches your sector. In 10–15 minutes, get a personalized readiness report highlighting gaps, risks, and next steps toward full EU compliance.

Each assessment is confidential, GDPR-compliant, and reviewed by our regulatory experts. Results are delivered instantly on-screen and by email.

GDPR-compliant

No spam, ever

10–15 minutes

## Choose Your Assessment

Three tailored evaluations, each built by QbD Group specialists for their respective regulatory framework.

Medical Devices

### EU MDR Readiness Assessment

Evaluate your medical device portfolio against EU MDR (2017/745) requirements — from technical documentation to post-market surveillance.

10–15 minutes

Pharmaceuticals

### EU Pharma Readiness Assessment

Benchmark your pharmaceutical operations against EU GMP, marketing authorization, and pharmacovigilance obligations.

10–15 minutes

Structural Heart & Coronary

### EU Cardiology Trials Readiness

Assess your structural heart and coronary clinical trial programs for EU MDR and CTR compliance.

10–15 minutes

## Need Guidance Beyond the Assessment?

Our regulatory affairs experts help pharmaceutical, medical device, and clinical trial teams achieve and maintain EU compliance every day.

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Source: https://qbdgroup.com/en/eu-readiness — © QbD Group. Quote freely with attribution and a link back.