Regulatory and technical resources of general interest to the medical device community are available here.
We mirror a subset of the FDA regulations and guidance documents here. This subset is of general interest to those companies producing medical devices with embedded software, and/or those who use software in the manufacture of medical devices.
From time to time, Intertech employees' articles are regularly selected for publication in industry periodicals on topics of interest to the industry. A collection of our article reprints are available by clicking the link above.
Webinars are occasionally offered at no cost to the industry. Click here to access archived webinars on various topics related to regulatory issues and medical device software.