ISMP National Medication Errors Reporting Program (MERP) has received several reports of patients who failed to...
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The FDA monitors reports of adverse events and other problems with medical devices and alerts health professionals and the public when needed to ensure proper use of devices and the health and safety of patients.
Suggestions for developing policies, procedures, and associated documents.
This article was published in the February 16, 2018 issue of Pharmacy Practice News.
This article appeared in the November 21, 2017 issue of Medical Device Business.
Assess the safety of systems and practices associated with up to 11 categories of medications.