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Medical device companies operate in a complex global regulatory environment with continually changing standards. NSF Health Sciences Medical Devices assists companies in navigating U.S. and international regulatory hurdles from product inception through product marketing. Our team of experts in the regulatory, scientific, analytical testing and compliance fields understands the industry and regulatory requirements to bring medical devices to market – and sustain them throughout their lifecycle.

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Recognized by regulatory agencies at the local, state, federal and international level, the NSF certification mark means that the product complies with all standard requirements.

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