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This document outlines the standard operating procedures for Beaumont physicians and laboratory personnel regarding the acquisition and sending out of non-Beaumont Health System research specimens
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How to fill out HIC REVIEW OF NON-BEAUMONT RESEARCH LABORATORY SEND OUT SPECIMENS

01
Begin by obtaining the HIC REVIEW OF NON-BEAUMONT RESEARCH LABORATORY SEND OUT SPECIMENS form from the appropriate source.
02
Fill in the title of your research project at the top of the form.
03
Include the names and affiliations of all researchers involved in the study.
04
Provide a detailed description of the research project, including its objectives and significance.
05
List all specimens that will be sent out, including type and quantity.
06
Specify the non-Beaumont research laboratory that will receive the specimens.
07
Include any relevant ethical considerations or approvals that have been obtained.
08
Sign and date the form, confirming all information is accurate.
09
Submit the completed form to the appropriate HIC review board for approval.

Who needs HIC REVIEW OF NON-BEAUMONT RESEARCH LABORATORY SEND OUT SPECIMENS?

01
Researchers conducting studies that involve sending specimens to non-Beaumont laboratories.
02
Those looking to comply with institutional review board requirements for ethical research practices.
03
Anyone involved in projects that require HIC review prior to specimen transfer.
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HIC REVIEW OF NON-BEAUMONT RESEARCH LABORATORY SEND OUT SPECIMENS is a review process that ensures compliance with ethical standards for handling and processing biological specimens sent to external laboratories for research purposes, particularly when these specimens do not originate from Beaumont Health facilities.
Researchers and investigators affiliated with Beaumont Health who are sending specimens to non-Beaumont laboratories for analysis must file the HIC review to ensure ethical considerations and regulatory compliance.
To fill out the HIC REVIEW OF NON-BEAUMONT RESEARCH LABORATORY SEND OUT SPECIMENS, researchers must complete a specific form detailing the nature of the specimens, the purpose of the research, consent from subjects, and the receiving laboratory's qualifications. This form should be submitted to the healthcare institution's Human Investigations Committee (HIC) for review.
The purpose of the HIC REVIEW is to protect the rights and welfare of research participants by ensuring that all specimens sent out for analysis adhere to ethical guidelines and legal regulations before being dispatched to external laboratories.
The information that must be reported includes the type of specimens being sent, the intended use of the specimens, consent details from research subjects, the identity of the non-Beaumont laboratory, and any potential risks involved in the research process.
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