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Synergy Health Concepts, Inc. IRB Protocol: Venous Obstruction in Neurodegenerative Disorders Research Registry Principal Investigator: John Joseph Hewitt, MD 24 Hour Telephone Number: 9492210129
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Start by gathering all necessary documents and information related to your research project.
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Access the SHC IRB protocol form on the appropriate website or platform.
03
Fill in the basic project details, including the title, principal investigator, and contact information.
04
Provide a clear and concise summary of your research objectives and methodology.
05
Detail any potential risks to participants and describe how you will minimize those risks.
06
Include information on participant recruitment and informed consent procedures.
07
Outline data management plans and how participant confidentiality will be protected.
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Review each section for completeness and accuracy before submission.
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Submit the completed protocol to the appropriate IRB committee for review.

Who needs shc irb protocol for?

01
Researchers conducting studies involving human subjects at SHC.
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Faculty members seeking approval for academic research projects.
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Students involved in research that requires ethical oversight.
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Healthcare professionals planning clinical trials or related studies.
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SHC IRB protocol is used to outline and manage the ethical review of research proposals involving human subjects to ensure compliance with regulatory and ethical standards.
Researchers and institutions conducting studies involving human subjects are required to file the SHC IRB protocol.
To fill out the SHC IRB protocol, researchers must complete the required application form with detailed study information, including objectives, methodology, and participant information, and submit it to the IRB for review.
The purpose of the SHC IRB protocol is to protect the rights and welfare of human subjects involved in research by ensuring thorough ethical review and oversight.
Information that must be reported includes the study's title, purpose, methodology, potential risks, informed consent process, and data management plans.
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