
FDA Reduces Regulatory Barriers
The FDA reduced regulatory barriers for remote patient monitoring devices during the COVID-19 crisis.
The FDA reduced regulatory barriers for remote patient monitoring devices during the COVID-19 crisis.
A set of Bluetooth LE vulnerabilities, collectively known as SweynTooth, brought attention to some straightforward attack vectors.
We have transitioned into an unprecedented landscape of remote work, here are some suggestions for staying user-centered.
Learn how to make your Human Factors (HF) usability studies less chaotic by investing in a small amount of planning and keeping some guidelines in mind.
There are several benefits associated with prototyping early in the design process
Part 3 of this Blog series focuses on a misconception that smaller is cheaper in medical products
Part 2 of Misconceptions of Miniaturization focuses on how the push to use smaller packaging can be counterproductive
The world seems to be preoccupied with miniaturization. Every device can be made smaller, and the first misconception is smaller is better.
Integrating technology readiness reviews into the product development process enables actionable processes that reduce project risk.
Learn more about how automated software testing augments other processes to dramatically improve product reliability, predictability, and productivity.
Agile methodology offers a more flexible approach and allows requirements to evolve to a more optimum solution for medical device development
What factors do you need to think about when building connected devices?