Objective To describe the extent of late adverse event reporting by manufacturers to the US Food and Drug Administration’s (FDA) Manufacturer And User Facility Device Experience (MAUDE) database as ...

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 ...

The best time to take vitamin B12 depends on why you are taking it and in what form. Learn the best timing for your needs.

There is no question that Mercedes has not had as successful a start to the electric age as it had hoped. The German carmaker ...

More than 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) ...

The movie is a telling look at the way we live now, when the gap between those struggling to pay the rent and those who are ...

A new study analyzing the FDA's Manufacturer and User Facility Device Experience database found that nearly one-third of medical device safety reports were not submitted within the 30-day timeframe or ...

Executives of Eacop Limited have revealed that 2026 may be the realistic timeline for the pipeline to start transporting oil ...

Nearly 10% of postmarket device safety reports in MAUDE were submitted over 6 months after the safety event occurred.

Investors would keep evaluating market metrics and significant developments to keep up with Pepe price prediction in the long ...

The riverboat captain is a storyteller. Captain Don Sanders shares the stories of his long association with the river — from ...

The rollout of new narrow-reef boring technology, which has the potential to boost platinum group metal (PGM) grades, lower ...