Dr. Thomas Gallagher has been through many tough conversations with patients. He remembers once standing in front of a patient and the patient's family, preparing to tell them about a mistake that had ...
Dublin, June 30, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course" training has been added to ResearchAndMarkets.com's offering ...
DUBLIN--(BUSINESS WIRE)--The "AI in Pharmacovigilance Training Course (Nov 19, 2025)" training has been added to ResearchAndMarkets.com's offering. This course will provide a comprehensive ...
This article appears in the February 2013 edition of Patient Safety Monitor. Mistakes happen. Many times when mistakes happen in hospitals, the hospital's system a nd process design has at least in ...
The authors explore the potential value of providing critical incident stress debriefing for health professionals involved in adverse patient safety events and the instances in which this could be ...
The U.S. Food and Drug Administration is now providing real-time, daily publication updates on adverse event data from its reporting system. In an effort to modernize and provide transparency on ...
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