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Department of Veterans Affairs Veterans Health Administration Washington, DC 20420VHA DIRECTIVE 1088 Transmittal Sheet October 7, 2015COMMUNICATING TEST RESULTS TO PROVIDERS AND PATIENTS 1. REASON
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How to fill out VHA Directive 1088:

01
Read through the entire VHA Directive 1088 document to familiarize yourself with its content and purpose.
02
Understand the specific requirements and guidelines stated in the directive, such as the forms to be completed, necessary information to provide, and any supporting documents needed.
03
Gather all the required information and documents before starting to fill out the directive.
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Begin by filling out the header section of the VHA Directive 1088 form, which includes personal or organizational details such as name, contact information, and affiliation.
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Follow the instructions provided in the directive to complete each section of the form accurately and thoroughly. Pay attention to any specific formatting or layout instructions mentioned.
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Provide all the necessary information, ensuring it is up-to-date and relevant to the purpose of the directive.
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Double-check the completed form for any errors, missing information, or inconsistencies. Make any necessary corrections before submitting it.
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Review the entire VHA Directive 1088 form once again to ensure that all sections have been properly filled out and all required information has been provided.
09
Date and sign the completed form, as indicated in the directive, to certify its authenticity and your agreement to comply with the directive's guidelines.
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Keep a copy of the filled-out VHA Directive 1088 form for your records.

Who needs VHA Directive 1088:

01
Any individual or organization within the Veterans Health Administration (VHA) that is responsible for developing and implementing programs related to research and development activities.
02
VHA facilities or medical centers that engage in research activities or receive funding for research efforts.
03
Researchers, scientists, and other personnel involved in conducting or overseeing research projects within the VHA.
04
VHA staff members responsible for ensuring compliance with research-related regulations, policies, and guidelines.
05
Individuals or organizations seeking to understand the specific requirements and guidelines for conducting research within the VHA.
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VHA Directive 1088 refers to the policy issued by the Veterans Health Administration (VHA) that outlines the requirements for reporting adverse events and ensuring patient safety.
All healthcare facilities and providers within the VHA network are required to adhere to VHA Directive 1088 and file reports as necessary.
VHA Directive 1088 can be filled out by following the guidelines and instructions provided in the directive document, which includes reporting requirements, forms, and contact information.
The purpose of VHA Directive 1088 is to improve patient safety, enhance transparency in reporting adverse events, and facilitate learning from errors to prevent future occurrences.
Information that must be reported on VHA Directive 1088 includes details of adverse events, patient harm, root causes, corrective actions taken, and follow-up plans.
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