Get the free IRB Form C-1 - brynmawr

This form is used by primary investigators at Bryn Mawr College to document the review status of research projects involving human subjects, detailing whether the project qualifies for exempt, expedited,

How to fill out irb form c-1

How to fill out IRB Form C-1

1. Begin by gathering all necessary documents related to your research project.
2. Provide a clear title for your research study at the top of the form.
3. Fill in your contact information, including name, email, and phone number.
4. Describe the purpose of the research in a concise paragraph.
5. Identify the research subjects and explain the recruitment process.
6. Outline the methods and procedures to be followed during the study.
7. Include information about any potential risks to participants and how they will be mitigated.
8. Specify the timeline for the study and any critical deadlines.
9. Review your responses for clarity and completeness before submitting.
10. Submit the completed IRB Form C-1 to the appropriate Institutional Review Board.

Who needs IRB Form C-1?

1. Researchers conducting studies involving human subjects.
2. Faculty members undertaking research projects within an academic institution.
3. Graduate and undergraduate students seeking to gather data as part of their thesis or dissertation.
4. Any individual or group involved in research requiring ethical review.

People Also Ask about

How to fill an IRB form?

Before completing the IRB application form, you must know: • The identity of all of the investigators who will be working on the project; • Who will be recruited to participate and how they will be recruited; • Where the research will be conducted; • What data will be collected and what will happen to that data; • How

How long does it take to get an IRB approval?

Projected wait times are approximately 24 months for refugee claims and 12 months for refugee appeals.

Is it hard to get IRB approval?

There are three (3) types of review paths for an IRB application: Full Board, Expedited, and Exempt.

How long is the wait for IRB?

Under 45 CFR 46.103, the IRB must review and approve all non-exempt human subject research. Failure to obtain IRB approval before conducting research could result in the researcher being unable to use data and other information collected through the research process.

What are the different types of IRB forms?

Submit all materials required for IRB review (e.g., intervention materials, investigator brochures for device or drugs, instruments, protocol, informed consent, information sheet, recruitment). Use the appropriate informed consent template (expedited and full board studies only).

Is IRB approval hard to get?

If your study is more than minimal risk, it will be harder for you to get IRB approval. You will need to justify why you are running the study. Less common types of risk for psychology studies are social, physical, and financial.

For pdfFiller’s FAQs

What is IRB Form C-1?

IRB Form C-1 is a form used by Institutional Review Boards (IRBs) to review and approve research involving human subjects, ensuring that ethical standards are met.

Who is required to file IRB Form C-1?

Researchers conducting studies involving human subjects or any entities seeking ethical review of their research proposals are required to file IRB Form C-1.

How to fill out IRB Form C-1?

To fill out IRB Form C-1, researchers must provide detailed information about the study's purpose, methodology, participant recruitment, informed consent processes, and any potential risks to participants.

What is the purpose of IRB Form C-1?

The purpose of IRB Form C-1 is to facilitate the ethical review process by providing IRBs with essential information about the research study, enabling them to assess potential risks and ethical considerations.

What information must be reported on IRB Form C-1?

IRB Form C-1 must report information including the research objectives, study design, participant demographics, potential risks and benefits, informed consent process, and contact information for the principal investigator.