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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EMAS certification with Kiwa: reduce your environmental impacts, engage employees and boost your reputation.Show
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ISO 37001 Anti-bribery Management Systems Certification with Kiwa: prevent, detect and address bribery to build trust in your brand and boost your business.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