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The U.S. Food and Drug Administration (FDA) is restricting the use of Keytruda and Tecentriq for patients with locally advanced or metastatic uro...
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Joint Commission Proposes Changes to National Patient Safety Goal Related to Anticoagulant Therapy
06/20/2018The Joint Commission is proposing new and revised requirements under National Patient Safety Goal (NPSG) 03.05.01, Reducing Harm from Anticoagula...
- The Joint Commission
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The U.S. Department of Health and Human Services (HHS) has extended the deadline for compliance with the requirements under the Federal Policy fo...
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The FDA continues to evaluate information from several sources and based on new information, the Endologix AFX with Strata device is at greater risk f...
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The Joint Commission has published a new FAQ addressing the role of residents, enrolled in graduate medical education program,s in writing orders...
- The Joint Commission
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The U.S. Food and Drug Administration has announced that they are aware of at least 43 patients with reported adverse events after receiving eye ...
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The Joint Commission (TJC) has announced that effective this month it is changing its survey process for assessing the culture of safety in hospi...
- The Joint Commission
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The Joint Commission has issued a standards FAQ clarifying their position on documentation requirements for home care organizations. Acc...
- The Joint Commission
- Home Health
The U.S. Food and Drug Administration (FDA) has released draft guidance “Humanitarian Device Exemption (HDE) Program” to answer commo...
- Food and Drug Administration
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The Centers for Disease Control and Prevention (CDC) and state health departments are investigating hepatitis A outbreaks in multiple states amon...
- Centers for Disease Control and Prevention
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According to the U.S Centers for Disease Control and Prevention (CDC), the United States 2017–18 influenza season (October 1, 2017–Ma...
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