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OFFICE of RESEARCH COMPLIANCE Quality assurance ORC-QA Institutional REVIEW BOARD IRB Protocol Synopsis Form for Research Involving Surveys IRB ALL research involving human subjects requires review and consideration by the RVU Office of Research Compliance Protection ORC-QA and the RVU Human Investigations Review Board IRB. Contact ORC-QA office for help in determining whether the project will need a HIPAA Waiver or Authorization Addendum to the Consent document. If you believe that this...
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Step 1: Start by obtaining the protocol synopsis form from the appropriate authority or organization.
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Step 2: Fill in the required personal information, such as your name, contact details, and affiliation.
03
Step 3: Provide a brief title for your protocol synopsis that effectively summarizes the research or study.
04
Step 4: Indicate the objectives, purpose, or aim of your study in a clear and concise manner.
05
Step 5: Describe the methodology or research design you will be using, including any data collection methods.
06
Step 6: Mention the expected outcomes or results you anticipate from your study.
07
Step 7: Specify any ethical considerations or measures you will take to ensure the safety and well-being of participants, if applicable.
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Step 8: If required, include a budget or financial plan for your study.
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Step 9: Review the completed form for accuracy, ensuring all necessary information has been provided.
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Step 10: Submit the protocol synopsis form to the designated authority or organization as per their instructions.

Who needs protocol synopsis form for?

01
Researchers conducting scientific studies or clinical trials usually need to fill out a protocol synopsis form.
02
Academic institutions, research organizations, or regulatory bodies may require researchers to submit this form.
03
Individuals or teams seeking funding or ethical approval for their research may also need to complete a protocol synopsis form.
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Protocol synopsis form is used to provide a brief overview of a research study or clinical trial.
Researchers or sponsors conducting a research study or clinical trial are required to file protocol synopsis form.
Protocol synopsis form can be filled out by providing information such as study title, objectives, study design, methods, and enrollment criteria.
The purpose of protocol synopsis form is to give a snapshot of the key aspects of a research study or clinical trial.
Information such as study title, objectives, study design, methods, and enrollment criteria must be reported on protocol synopsis form.
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