Medical Devices… and More
The medical device industry is one of the most vibrant and important drivers of the health care economies. Regulations to ensure the safety of devices and in vitro diagnostics are evolving rapidly in the international arena.
In these series of videos, users with a basic knowledge of biomedical science and regulatory structures will explore in depth the policies and practices of regulatory research, review, and management for these product classes.
They will be able to integrate this knowledge with scientific principles related to the development of experimental protocols and testing paradigms, in order to plan, critique and provide direction to complex device programs.
Recorded trainings and discussions
Click an event to view recordings & materials
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Harmonizing Medical Device Regulation
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Medical Devices 2021:
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Spring 2019 – Los Angeles, CA
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