Checklist
EU MDR Compliance Checklist
A complete step-by-step checklist covering every EU MDR compliance requirement — from appointing your EU AR to post-market surveillance.
- 6 compliance phases
- 40+ checklist items
- All device classes
- EUDAMED registration steps
- Labelling requirements
Guide
EUDAMED Readiness Guide
Everything you need to know about EUDAMED mandatory registration — who must register, the 5 steps, key deadlines and what happens if you miss them.
- 28 May 2026 deadline explained
- Who must register table
- 5-step registration process
- Full deadline timeline
- SRN acquisition guide
Roadmap
CE Marking Roadmap
A visual roadmap to CE marking for every device class — timelines, steps, Notified Body requirements and the most common mistakes to avoid.
- Class I, IIa, IIb, III pathways
- Realistic timelines per class
- Notified Body process explained
- Common mistakes to avoid
- Technical documentation guide
Need personalised compliance guidance?
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