Per federal regulations, University and affiliate researchers must notify the IRB of unanticipated problems that involve risks to participants or others (henceforth referenced as Unanticipated ...

Please provide your email address to receive an email when new articles are posted on . The FDA Adverse Event Reporting System will now host daily publications, instead of quarterly. The agency’s goal ...

MANKATO — Newly released data showed south-central Minnesota had an uptick in adverse events, including serious injuries, among patients at health care facilities over a one-year period during the ...

Clinical trials utilize multiple methods of tracking, categorizing, and assessing any side effects at each trial stage. A negative side effect during clinical trials, whether expected as a potential ...

MANKATO — An annual report released in late June by the Minnesota Department of Health reveals that hospitals and ambulatory surgery centers reported a smaller increase in mistakes than the previous ...

The Law of Mass action predicts that all adverse drug reactions are related to the concentration of the drug at the site of ...

The Journal of Clinical Oncology podcast, hosted by Dr. Davide Soldato, presents analyses and discussions centered on the latest findings published in ASCO’s esteemed Journal of Clinical Oncology.