Medical Device Network on MSN9d
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 ...
MedTech Dive4d
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 ...
Dermatology Advisor1d
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.
Medscape3d
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) ...
Targeted Oncology2d
Optimizing Frontline TKI Therapy in Advanced uHCC: Managing Adverse Events
An expert discusses how in the first-line (1L) treatment of advanced unresectable hepatocellular carcinoma (uHCC) with tyrosine kinase inhibitors (TKIs) such as lenvatinib or sorafenib, proactive ...
Targeted Oncology2d
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 ...