In brief Mobile applications have attracted much attention recently (in the future, “apps”). Some of these applications aren’t very useful, and they don’t have a lot […]

In brief In new medications, the FDA’s clearance procedure is designed to provide consumers confidence that a medical device will be safe and effective in its […]

In brief The content and quality determine the value of medical device registries (MDRs); MDRs must have a strong and suitable structure to achieve their goals. […]

In brief The reviewing process, in theory, may considerably enhance work by allowing many experts in the subject to provide input. Indeed, actual data shows that […]

In brief  The miniaturization, complexity, proliferation, and accessibility of technology enable capturing inaccessible events in Parkinson’s disease (PD). However, additional information has not resulted in a […]

In brief  Clinical trial monitoring services are critical for medical progress. Medical technology advancements in recent decades have resulted in earlier and more accurate diagnoses, more […]

In brief  Developing guidelines based on a thorough analysis of the data found in diagnostic research literature searches reports, methodological standards for judging diagnostic research, techniques […]