Get the free Carilion IRB Application (Version 1.8)

Carilion IRB Application (Version 1.8) 1.0General Information*Please enter the full title of your study:: A Comparison of the Effectiveness of Telepsychiatry with a Randomized Waitlist Control Utilizing

How to fill out carilion irb application version

How to fill out carilion irb application version

1. Download the Carilion IRB application version from the Carilion website.
2. Read the instructions carefully before starting the application.
3. Fill in the project title and abstract in the designated fields.
4. Provide detailed information about the study's purpose and methodology.
5. Include information about the main researchers and their qualifications.
6. Specify the funding sources, if any.
7. Fill out the participant recruitment section, addressing inclusion and exclusion criteria.
8. Outline the risks and benefits of the study clearly.
9. Attach any supplementary documents, such as consent forms and survey instruments, as required.
10. Review the application thoroughly for completeness and accuracy.
11. Submit the application through the designated online portal or email, per Carilion's guidelines.

Who needs carilion irb application version?

1. Researchers planning to conduct studies involving human subjects.
2. Academic institutions partnering with Carilion.
3. Organizations seeking ethical approval for clinical trials or health-related research.
4. Employees of Carilion who are involved in research projects.

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What is carilion irb application version?

The Carilion IRB application version refers to the specific iteration or release of the Institutional Review Board application used by Carilion to review research protocols.

Who is required to file carilion irb application version?

Any researcher or investigator conducting a study involving human subjects that requires ethical review must file the Carilion IRB application version.

How to fill out carilion irb application version?

The Carilion IRB application version can be filled out by following the guidelines provided by the IRB office, which typically includes sections for study methodology, participant information, and ethical considerations.

What is the purpose of carilion irb application version?

The purpose of the Carilion IRB application version is to ensure the protection of human subjects involved in research and to comply with federal regulations and institutional policies.

What information must be reported on carilion irb application version?

Information required on the Carilion IRB application version includes study objectives, methods, participant recruitment strategies, informed consent processes, and potential risks to participants.