However, "two participants experienced serious adverse events of AF requiring cardioversion," or treatment to get a heart back to a normal rhythm. The company said that the rate of patients who ...

Nearly a third of medical device adverse events were not submitted to the FDA within a 30-day regulatory window, with most late reports filed more than six months after manufacturer notifications ...

Dr. Nisha Acharya got a letter from the National Institutes of Health terminating her grant to study the safety and ...

Applying for an NIH grant can be a daunting process. NIH grants are highly competitive and require a careful strategy in order to build a winning proposal. Applicants who have strong and innovative ...

Objectives: To conduct a multicentre study on adverse event and near miss reporting in the NHS and to explore the feasibility of creating a national system for collecting these data. Design: ...

A health care professional can submit an AEFI report. If you are a vaccine recipient who has recently been vaccinated and have experienced an adverse event following immunization, please ask your ...

Stella, as she is known, is a Nurse Manager at the National Institute for Health and Care Research (NIHR) Manchester Clinical Research Facility (CRF) at Wythenshawe Hospital, part of Manchester ...

and preventability of adverse drug events (ADEs) and medication errors is crucial to improving the quality of health care delivery. ADEs, potential ADEs, and medication errors can be collected by ...

Samples of successful pilot proposals can be found in the "Samples & Templates" section below. Human Participants Protections Education for Research Teams: the online training course required for all ...