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The medical device industry is the most highly regulated industry in the world. Intertek’s medical industry experience and expertise coupled with our ability to test to a variety of international requirements simultaneously enables us to get your project done faster without sacrificing quality. Intertek can perform FDA 510(k) reviews, electrical safety certification including CE Marking, testing to the MDD and IVDD, risk analysis, EMC and performance testing. Our global reach and knowledge of international requirements will ultimately help you as a manufacturer get your product to market faster.
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