Learn all you need to know about the European Medical Devices Regulation (EU MDR), which becomes mandatory for medical device producers on May 26, 2021.
The EU MDR replaces the previous Medical Device Directive (EU MDD) and Active Implantable Medical Device Directive.
EU MDR changes how medical devices are defined, how devices are classified for risk, and creates a new labeling system. The regulation also includes certain substance content requirements.
Learn exactly what the EU MDR is and what you need to know to comply. Plus, learn about our EU MDR solution online at [ Ссылка ]
What is the EU Medical Devices Regulation (MDR)?
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medical devicesmedical devicemdreu mdreuropean medical devices regulationmedical devices regulationmddmedical devices directiveIVDRin vitro diagnostic medical devicesactive implantable medical devicesMDDAIMDIVMDDengineeringmanufacturingelectrical engineeringdesign engineeringquality engineeringenvironmental engineeringquality assurancequality managementmaterials managementregulatory complianceenvironmental regulationssubstanceschemicals
