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  • The second MDR Corrigendum published by the European Council: the main changes proposed.
    29 November 2019

    IOn November 25, 2019 the European Union Council published the second corrigendum to the EU Medical Devices Regulation 2017/745 (MDR) which includes corrections and clarifications. Among the changes, the most relevant is the four additional years for Class I devices’ manufacturers to conform to the requirements.

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  • Kiwa obtains the ACCREDIA accreditation for tests carried out in the New Italian Plastic Lab
    25 November 2019

    Kiwa has recently obtained the extension of the ACCREDIA LAB n°0001L accreditation for the tests carried out in the Plastic dedicated testing facility in Bologna, Italy.

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  • Kiwa member of Hydrogen Europe
    22 November 2019

    We are proud that we are now member of Hydrogen Europe, the association that represents the European industry, national associations and research centres active in the hydrogen and fuel cell sector.

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