Download our EU MDR general safety and performance requirements (GSPR) checklist to:
- Understand every requirement your business and device(s) must follow for EU-compliant medical device safety and performance
- Take controlled step-by-step action to get compliant
- Pinpoint gaps in your medical device quality management system and satisfy your EU notified body inspector
Complete the form to the right to get started!
What you'll get:
4-part XLSX checklist
Access a comprehensive and ordered Excel checklist to work your way through your GSPR demands
Itemized action points
From referencing documents in your Design History File (DHF) to ticking off device requirements, work your way through the checklist to plug gaps and maximize compliance
Annex-specific requirements list
Understand the requirements by annex and chapter and build a comprehensive record of documentation to prove compliance to your inspector