Supply Chain
Long wait times, crowded waiting rooms, and frustrated staff are often symptoms of inefficient workflows driven by physical space constraints.…
The market for medical device outsourcing and contract manufacturers as brand owners is expected to increase to more than $12 billion by 2018.
The U.S. Food and Drug Administration announced it has approved the first gel sealant that can be used for preventing leakage of fluid through the incision in a patient's cornea after cataract surgery with intraocular lens placement in adults.
Reducing the number of intensive care unit beds could increase care quality while reducing overall healthcare costs, playing into the idea of demand elasticity, according to an article in the Journal of the American Medical Association.
The U.S. Food and Drug Administration announced a recall on Boulder, Colo.-based Covidien's Puritan Bennet 840 Series ventilator.
Employees from the secretive Google X research group have met with members from the U.S. Food and Drug Administration who oversee and regulate eye devices and diagnostics for heart conditions, according to a Bloomberg report.
Crystal Lake, Ill.-based Centegra Health System selected Mundelein, Ill.-based Medline Industries to serve as its preferred distribution partner for the next three years, according to a news release.
The total global anesthesia and respiratory devices market is expected to be worth $12.7 billion by 2015, according to a new report published by MarketsandMarkets.
The medical and surgical instrument manufacturing industry is expected to be valued at $61 billion by 2017, according to a Research and Markets report.
The U.S. Food and Drug Administration approved 17 percent fewer "first-of-a-kind" drugs in 2013 than in 2012, according to an ABC News report.
The U.S. Food and Drug Administration has cleared Waltham, Mass.-based EarlySense's EarlySense 2.0 bedside monitoring system, according to a news release by the company.