EU finalizes 1-year MDR application delay
Due to the COVID-19 outbreak, the EU has postponed the date of application of the EU Medical Devices Regulation by one year. The Medical Devices Directives transitional period has also been extended.
Existing natural gas infrastructures can be made suitable for the distribution of hydrogen relatively easily. Kiwa’s approval requirement (AR) 214, focused on hydrogen, contains the specific requirements components in networks must meet.
Due to the COVID-19 outbreak, the EU has postponed the date of application of the EU Medical Devices Regulation by one year. The Medical Devices Directives transitional period has also been extended.
Kiwa has launched a quality mark for the review of COVID-19 Preventive measures for organizations that wish to have their COVID-19 measures tested against the applicable (inter)national requirements and any additional guidelines.
Being a leader in quality and reliability also includes compliance, proper conduct and living up to a high moral standard. To ensure we do, Kiwa is working according to a Conduct and Compliance framework.
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