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Principal Investigator Information Sheet Please provide information about the Investigator and the Research Site: 1. Principal Investigator Name: 2. Does the PI have an obligation to use another IRB
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How to fill out protocol information sheet
How to Fill Out Protocol Information Sheet:
01
Start by gathering all the necessary information for the protocol information sheet. This may include details about the study or project, participant information, and any specific procedures or guidelines that need to be followed.
02
Begin filling out the sheet by providing the basic information about the study, such as the title and purpose. This helps to give an overview of what the protocol is about.
03
Include details about the study participants, such as their demographic information, inclusion and exclusion criteria, and any relevant medical history. This helps to ensure that the study is tailored to the specific population being targeted.
04
Next, outline the specific procedures that will be performed during the study. This can include details about the intervention or treatment, data collection methods, and any follow-up procedures.
05
It is important to include any potential risks or benefits associated with participating in the study. This helps to inform the participants and ensure their safety throughout the research process.
06
Provide clear instructions on how to obtain informed consent from participants. This includes explaining the purpose of the study, potential risks and benefits, and ensuring that participants have the opportunity to ask any questions they may have.
07
Lastly, make sure to include contact information for the principal investigator or study coordinator. This allows participants to reach out with any concerns or questions they may have throughout the course of the study.
Who Needs a Protocol Information Sheet:
01
Researchers or investigators conducting a study or project that involves human participants will need a protocol information sheet. This document outlines the essential details of the study and ensures that all necessary information is provided to participants.
02
Ethical review boards or institutional review boards (IRBs) may also require researchers to provide a protocol information sheet. This helps to ensure that participant safety and informed consent guidelines are followed.
03
Participants in the study or project will also benefit from having a protocol information sheet. It allows them to fully understand the purpose, procedures, risks, and benefits associated with their involvement, helping them to make an informed decision about participating.
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What is protocol information sheet?
Protocol information sheet is a document that contains detailed information about a protocol or research study.
Who is required to file protocol information sheet?
Researchers, institutions, or organizations conducting a research study are required to file protocol information sheet.
How to fill out protocol information sheet?
Protocol information sheet can be filled out by providing information about the study design, objectives, methods, participants, and any potential risks or benefits.
What is the purpose of protocol information sheet?
The purpose of protocol information sheet is to provide transparency and ensure that research studies are conducted ethically and in compliance with regulations.
What information must be reported on protocol information sheet?
Information such as study title, investigators, study design, methods, and ethical considerations must be reported on protocol information sheet.
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