Module 19: Regulation of In Vitro Diagnostic Medical Devices
13/04/2023
IVD Risk Management
Risk Management is important in IVDD Risk Management is essential in IVDR
‘Manufacturers shall establish, implement, document and maintain a risk management system’ – IVDR Art. 10, Annex I part 3
IVDD 98/79/EC
2017/746/EU
Reference to ‘risk’ ....
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Take home messages
Well defined systematic process to determine product safety and effectiveness
Embedded throughout QMS/ ISO 13485 / MDSAP Critical for ongoing compliance to the IVD Regulation Appropriate to product type and risk Requires collective collaboration of expertise Can be a very useful tool
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