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FOR IRB USE ONLY APPROVED BY: IRB01 IRB ID #: 201504731 APPROVAL DATE: 05/15/18 EXPIRATION DATE: 05/10/19INFORMED CONSENT DOCUMENT Project Title: Neoadjuvant Intraluminal Injection of Imogene Laherparepvec

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How to fill out approved by irb-01

1. To fill out the approved by irb-01 form, follow these steps:
2. Write the title of the research project at the top of the form.
3. Provide details about the researcher, including name, contact information, and affiliation.
4. Specify the purpose of the research and briefly describe the methodology.
5. Indicate the anticipated duration of the project and any potential risks involved.
6. Include information about the subjects or participants of the research study.
7. Highlight any measures taken to ensure informed consent and protection of the participants' privacy.
8. Include a description of the potential benefits that may arise from the research.
9. Provide a list of references or sources used to support the research study.
10. Seek approval from the Institutional Review Board (IRB) by submitting the filled-out form.
11. Wait for the IRB's decision and follow any suggested modifications or guidelines if necessary.

Who needs approved by irb-01?

1. Researchers who are conducting research studies involving human subjects need to have their projects approved by irb-01. This includes researchers from academic institutions, medical centers, and other organizations conducting studies that involve human participants.

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What is approved by irb-01?

Approved by irb-01 refers to research projects or studies that have been reviewed and approved by the Institutional Review Board (IRB) at a specific institution.

Who is required to file approved by irb-01?

Researchers, scientists, or institutions conducting research involving human subjects are required to file for approval by irb-01.

How to fill out approved by irb-01?

To fill out approved by irb-01, researchers need to provide detailed information about the research study, the methods used, the potential risks to participants, and how participant confidentiality will be protected.

What is the purpose of approved by irb-01?

The purpose of approved by irb-01 is to ensure that research involving human subjects is conducted ethically, with participant safety and well-being as the top priority.

What information must be reported on approved by irb-01?

Information such as the study protocol, informed consent forms, data collection methods, potential risks and benefits to participants, and how participant confidentiality will be maintained must be reported on approved by irb-01.