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Department of Veterans Affairs Veterans Health Administration Washington, DC 20420VHA HANDBOOK 1108.01 Transmittal Sheet November 16, 2010CONTROLLED SUBSTANCES (PHARMACY STOCK)1. REASON FOR ISSUE.
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Who needs VHA Directive 1108 01:

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Healthcare providers: VHA Directive 1108 01 is primarily designed for healthcare providers within the Veterans Health Administration (VHA). This directive serves as a guide for managing specific aspects, protocols, or procedures related to healthcare delivery within the VHA system.
02
VHA administrators: VHA Directive 1108 01 is also important for VHA administrators who are responsible for implementing and ensuring compliance with the policies and procedures outlined in the directive. It provides them with a framework to standardize healthcare practices and promote consistency across VHA facilities.
03
Veterans and their families: While VHA Directive 1108 01 primarily applies to healthcare providers and administrators, it indirectly impacts veterans and their families. The directive aims to enhance the quality of care and improve patient outcomes, making it relevant to those receiving healthcare services within the VHA system.
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VHA Directive 1108 01 is a directive issued by the Veterans Health Administration that outlines requirements and procedures related to the reporting of adverse events.
All healthcare facilities and providers within the Veterans Health Administration are required to file VHA Directive 1108 01.
VHA Directive 1108 01 can be filled out by following the specific instructions provided in the directive document, which includes reporting requirements and procedures.
The purpose of VHA Directive 1108 01 is to ensure the timely and accurate reporting of adverse events within the Veterans Health Administration in order to improve patient safety and quality of care.
VHA Directive 1108 01 requires the reporting of any adverse events, near misses, or other quality concerns that may impact patient safety.
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