The Evolution of Medical Device Clinical Trials: Their Background and a Look Toward the Future
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.
