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The Evolution of Medical Device Clinical Trials: Their Background and a Look Toward the Future
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"The Evolution of Medical Device Clinical Trials: Their Background and a Look Toward the Future"
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Demonstrating the effectiveness and safety of new medical products is a critical part of the medical product development process and requires significant resources to accomplish.

Global regulatory affairs and compliance expert David Dills provides a comprehensive overview of the evolution of medical device clinical trials regulations and explains how in-depth knowledge of regulatory requirements and the application of rigorous clinical investigation processes can help companies accelerate the time it takes to bring new devices to the market.


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