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WELLESLEY COLLEGE IRB GUIDE Effective January 21, 2019, Revised June 26, 2020iiWellesley College IRB Guide, 1/21/2019 Revised Common Rule. 1.16.19 VersioniiiCONTENTS Summary of Revised Common Rule
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01
To fill out IRB review guidelines, follow these steps:
02
Read the guidelines carefully to understand the requirements and expectations.
03
Collect all the necessary information and documents related to your research project.
04
Begin the online application process by accessing the IRB review portal.
05
Provide the required information about the research project, such as title, abstract, and purpose.
06
Answer questions regarding the study design, methodology, participant recruitment, and informed consent process.
07
Upload any supporting documents, such as research protocols, surveys, or recruitment materials.
08
Review and confirm all the information provided before submission.
09
Submit the completed application and wait for the IRB review process to commence.
10
Respond promptly to any queries or requests for revisions from the IRB committee.
11
Once the review process is complete, address any required revisions or modifications.
12
Follow the approved guidelines and protocols while conducting the research project.
13
Keep all records and documentation related to the IRB review for future reference.

Who needs irb review guidelines?

01
Individuals or organizations involved in research projects that involve human participants need IRB review guidelines.
02
This includes researchers in academic institutions, medical professionals, pharmaceutical companies, social scientists, and anyone conducting research that could potentially impact human subjects.
03
IRB review guidelines ensure the protection of human participants' rights, welfare, and well-being during the research process.
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IRB review guidelines refer to the set of procedures and regulations established to ensure ethical review of research involving human subjects. These guidelines help protect the rights and welfare of participants.
Researchers and institutions that conduct studies involving human subjects are required to file IRB review guidelines.
To fill out IRB review guidelines, researchers typically need to complete an application form detailing their research proposal, informed consent processes, and any potential risks to participants.
The purpose of IRB review guidelines is to ensure that research complies with ethical standards and protects the rights and welfare of human participants.
Information that must be reported includes study objectives, methods, potential risks, benefits, consent processes, and plans for data management.
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