When it comes to medical treatment, medical devices and pharma, safety and health are of vital importance. Your customers expect the best possible treatment and you want to offer effective, efficient and high-quality care. Client safety demands active prevention of risks, while health authorities demand transparent, documented, traceable processes. Medical devices manufactured or traded in the EU must comply with EU legislation in the area of safety and health. This means they have to be conform to the pertaining product directives and must be CE marked. Kiwa's wide range of expert services helps you prevent risks and improve quality, safety and security.
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ISO 14001 Environmental Management Certification with Kiwa: reduce waste, gain customer trust and be competitive.Show
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Kiwa boasts a wide and in-depth experience as Notified Body from over 20 years in Medical Devices certification, with thousands of products already certified.Show
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