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Post-Market Radar Demo Booking  
Stay informed and compliant with Post-Market Radar – for maximum security in your post-market surveillance.  
Regulatory Radar Demo Booking  
The Regulatory Radar keeps you updated with the latest global medical technology and pharmaceutical industry regulations. Book your free demo now.  
Regulatory Intelligence Demo Booking  
Our Regulatory Intelligence SaaS keeps you up to date through regulatory monitoring and ensures company-wide compliance. Book your free demo now.  
Clinical Evaluation  
Pass approvals, audits, and reviews quickly and safely with legally compliant clinical evaluations. Thanks to our clinical affairs services.  
IVD Performance Evaluation Strategy  
We help you develop a targeted performance evaluation strategy that is optimally suited to the intended purpose of your in-vitro diagnostic medical devices.  
Usability Engineering  
Our free quick guide helps you implement the usability process in compliance with IEC 62366-1, avoid costly rounds of revisions, and successfully pass MDR and FDA audits.  
Biocompatibility Checklist  
Avoid delays in MDR approval: How to request biocompatibility data in accordance with ISO 10993-1:2025.  
Our Locations  
Where to Find Us: The Johner Institute is Represented Internationally at Several Sites in Europe and the USA  
Software & (IVD) Medical Devices with AI  
We help you to efficiently develop and successfully approve your software medical devices and IVD software – including AI-based medical devices.  
Risk Management  
Pass approvals, audits, and reviews quickly and easily with legally compliant risk management files and safe medical devices.  
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