MDSAP - The Medical Device Single Audit Program The International Medical Device Regulators Forum (IMDRF)External Link Disclaimer recognizes that a global approach to auditing and monitoring the manufacturing of medical devices could improve their safety and oversight on an international scale. <Detail>

CE marking Process, CE Certification Procedure Organizations and enterprises to obtain CE certification and are allowed to place CE marking on products need to follow the following requirements in order. Before you place the CE marking on a product, you need to know what the EU Directives apply to y <Detail>

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