UBS Group AG’s auditor Ernst & Young expressed an “adverse opinion” on internal controls over financial reporting related to ...

Nearly a third of medical device adverse events were not submitted to the FDA within a 30-day regulatory window, with most ...

The COVID-19 vaccine has prompted more than 10 times as many reports of adverse symptoms than the measles vaccine.

Although most manufacturer reports of medical device adverse events are reported on time, a considerable proportion are submitted late.