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 13485 Medical Devices Certification with Kiwa: ensure quality, build trust and comply with regulations in the medical devices sector.Show
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ISO 14001 Environmental Management Certification with Kiwa: reduce waste, gain customer trust and be competitive.Show
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ISO 27001 Information Security Certification with Kiwa: secure your information, build trust in your brand.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, providing all the necessary services to get complete answers and reliable information on medical devices certification services according to 93/42/EEC Directive.Show
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Kiwa offers to Organizations the opportunity to carry out electrical safety, electromagnetic compatibility and any functional test in its laboratories, with respect to the harmonized Standards.Show