MedTech Dive3d
Top device firms report safety data late: BMJ
BD, Medtronic and Abbott were among the top 10 device companies with the highest number of late reports to the FDA, the study ...
Medical Device Network on MSN8d
Nearly a third of FDA medical device adverse event reports filed late
A new study found that 9.1% of medical device AEs were reported to the FDA 180 days later than required over a three-year ...
Dermatology Advisor17h
Considerable Proportion of Medical Device Adverse Events Reported Late
Less than three-quarters of medical device-related adverse events are reported on time by their manufacturers.
Medscape2d
Heart Failure Care Outside of ICU Can Lower Cost
A protocol for transitioning patients with heart failure and a left ventricular assist device to a stepdown unit from the ICU ...
More than 1.2 million medical device side-effect reports not submitted within legal timeframe, analysis finds
More than 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) ...
The Cardiology Advisor17h
Hyperkalemia in Chronic Kidney Disease Increases Adverse Cardiovascular Events
In patients with CKD, hyperkalemia significantly increases risk for major adverse cardiovascular events and arrhythmia.
Targeted Oncology1d
Experience Managing irAEs Vital for Both Oncologists and Specialists
During a live event, James W. Smithy, MD, MHS, and other oncologists discussed how their experience with immune-related ...