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Page 1 of 2 IRB Supplemental Form C Request for Approval of Deception in Research Principal Investigator: Study Number: Study Title: Date Submitted: 1. Are the risks to subjects in this research greater

How to fill out irb supplemental form c

How to fill out irb supplemental form c?

1. Start by gathering all the necessary information and documents required for the form. This may include the name of the research project, the principal investigator's information, and any supporting documents.
2. Begin filling out the form by providing your personal information, such as your name, contact information, and institutional affiliation. Make sure to double-check the accuracy of this information before continuing.
3. Next, proceed to the section where you need to describe the research intervention or procedure. Clearly and concisely explain the purpose of the study, the specific interventions involved, and any potential risks or benefits to the participants.
4. In the following sections, include details about the recruitment and informed consent process. Describe how participants will be recruited, the steps taken to obtain informed consent, and any safeguards in place to protect privacy and confidentiality.
5. If applicable, provide information about any data collection methods or instruments used in the study. This may include surveys, interviews, or observations. Be sure to adequately explain these methods and address any potential risks or benefits associated with them.
6. Finally, review the completed form for any errors or missing information. Make sure that all sections have been appropriately addressed and that any required attachments or supporting documents have been included.
7. After completing the form, follow the specific submission instructions provided by the Institutional Review Board (IRB) or the organization overseeing the research. This usually involves submitting the form electronically or physically to the designated department.

Who needs irb supplemental form c?

1. Researchers conducting studies involving human participants may need to fill out an IRB supplemental form C. This form is typically required when additional information is needed that goes beyond what is covered in the main IRB application.
2. Researchers planning to implement interventions or procedures that involve potential risks, modifications to existing protocols, or any unique circumstances may need to complete this form. It allows the IRB to assess and approve these additional aspects of the research.
3. Investigators who want to make amendments to an existing research protocol may also be required to fill out an IRB supplemental form C. This ensures that any changes to the study are thoroughly reviewed and approved by the IRB before implementation.

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What is irb supplemental form c?

IRB supplemental form c is a document used to provide additional information for Institutional Review Board (IRB) approval of research involving human subjects.

Who is required to file irb supplemental form c?

Researchers conducting studies involving human subjects are required to file IRB supplemental form c.

How to fill out irb supplemental form c?

To fill out IRB supplemental form c, researchers need to provide detailed information about the additional aspects of their study that were not covered in the initial IRB application.

What is the purpose of irb supplemental form c?

The purpose of IRB supplemental form c is to ensure that the research involving human subjects is conducted ethically and in compliance with regulations.

What information must be reported on irb supplemental form c?

Information such as changes in study protocol, recruitment strategies, consent forms, and any potential risks to participants must be reported on IRB supplemental form c.

How do I make changes in irb supplemental form c?

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