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The International Patient Safety Goals (IPSG) were developed in 2006 by the Joint Commission International (JCI). The goals were adapted from the JCAHO's National Patient Safety Goals. [1] Compliance with IPSG has been monitored in JCI-accredited hospitals since January 2006. [1]
Patient safety work product includes any data, reports, records, memoranda, analyses (such as root cause analyses), or written or oral statements (or copies of any of this material), which are assembled or developed by a provider for reporting to a PSO and are reported to a PSO; or are developed by a patient safety organization for the conduct ...
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Robert M. Wachter, a prominent expert in patient safety, who coined the term hospitalist and is considered the academic leader of the field of hospital medicine. Wachter is now chair of UCSF's Department of Medicine. Peter Walter, molecular biologist and biochemist, Shaw Prize (2014) and Lasker Award (2014)
Level 2 Hospitals in Philippines: Building upon the foundational requirements of Level 1, these hospitals provide departmentalized specialty services, intensive care units (ICU), respiratory therapy, advanced tertiary clinical laboratory services, and enhanced imaging capabilities.
As a result, patient safety has emerged as a distinct healthcare discipline, supported by an immature yet developing scientific framework. There is a significant transdisciplinary body of theoretical and research literature that informs the science of patient safety, [3] with mobile health apps becoming an increasingly important area of study. [4]
A patient involvement group, Patients for Patient Safety, built networks of patients’ organizations from around the world, through regional workshops. A patient safety taxonomy was developed to classify data on patient safety problems. Prevalence studies conducted on patient harm in ten developing countries.
The role of therapeutic goods regulation is designed mainly to protect the health and safety of the population. Regulation is aimed at ensuring the safety, quality, and efficacy of the therapeutic goods which are covered under the scope of the regulation. In most jurisdictions, therapeutic goods must be registered before they are allowed to be ...