The FDA's oversight is crucial as it covers various aspects of the medical device industry, including the path to market, post-market surveillance, device recalls, and key definitions. Medical devices are categorized into Class I, II, and III, with each class subject to different levels of regulation. HTM professionals in healthcare organizations play an essential role in ensuring compliance with FDA guidelines to manage medical devices safely and efficiently, benefiting patient care outcomes.

201 - Overview of the FDA

The key to building a strong HTM industry is building a strong HTM community.  We encourage you to share, interact, and network through local, regional, and national groups.  We strive to enhance academic offerings, create a pipeline for the next generation of HTM professionals, and provide opportunities for those already rooted in the industry to grow.

New tracks tagged #clinical engineering