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3rd Northern German Dialogue: Software in Medicine Fechnology

“Risk management for medical products 2.0″ is the key topic of the symposium, taking place in Hamburg 25-26 September 2014.

Organised by PROSYSTEM and Life Science Nord, the industry meeting at Mövenpick hotel will feature these topics:
• Regulatory requirements for software
• Approval of medical software (EEA & USA)
• Development of medical software
• Risk management and serviceability
• Clinical evaluation and validation
• New requirements for software in medical technology

In focus: EN ISO 14971

This year, the symposium will thus focus on current changes to EN ISO 14971 and related interfaces. Manufacturers, representatives from public authorities and industry partners will meet in Hamburg to gather insights on latest trends and developments, discuss open questions and best practices, and to give an outlook on the changes the medical industry may encounter in coming years, also in regard to the planned introduction of the European Medical Device Regulation.

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