Supply Chain
Long wait times, crowded waiting rooms, and frustrated staff are often symptoms of inefficient workflows driven by physical space constraints.…
This week, the FDA released a draft guidance document designed to help medical device makers better understand the agency's stance on patient access to device data.
A new in-vitro fertilization technique designed to reduce the risk of women passing on hereditary diseases to their children proved promising in a study done by researchers at Britain's Newcastle University in Tyne and Wear.
Medford, Mass.-based Seventh Sense Biosystems developed a device the size of a walnut to eliminate the fear, pain and inconvenience associated with drawing blood.
Philadelphia-based Prairie Dog Tech announced the launch of a new image capturing device that provides immediate access to real time photos of endoscope cleaning sinks.
The FDA recently approved a software-controlled bedside device that uses a wearable pad to keep the forehead cool, allowing users to fall to sleep faster.
The FDA's pattern of approving high numbers of generic drug applications to increase market competition has slowed in recent months. The latest release of raw data on Tuesday showed an all time high amount of complete response letters, or rejections,…
A new bill introduced to Congress on Wednesday would require physicians to report potentially serious problems with medical devices to the FDA, according to The Wall Street Journal.
The FDA eliminated some paperwork physicians must complete to obtain experimental drugs for patients with life-threatening illnesses that don't respond to standard therapies.
Medical supply website AvaCare Medical provides bed-bound patients access to tens of thousands of medical supplies not always covered by insurance.
Today the Michael J. Fox Foundation for Parkinson's Research announced a data challenge to accelerate development and testing of new therapies for Parkinson's disease.