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CONTINUING REVIEW OF PREVIOUSLY APPROVED RESEARCH For Full Review Research HENDRIX COLLEGE HUMAN SUBJECTS REVIEW Board U. S. Department of Health and Human Services regulations for the protection

How to fill out continuing review form

How to fill out continuing review form

1. Start by reviewing the continuing review form and familiarize yourself with its sections.
2. Fill out the basic information section, which includes details such as the study title, principal investigator, and study team members.
3. Provide a summary of the study progress since the last review. Include any amendments, adverse events, or changes to the study protocol.
4. Answer any specific questions asked in the continuing review form. These questions may vary depending on the nature of the study.
5. Submit any relevant documentation required along with the form, such as updated study protocols or participant consent forms.
6. Review the completed form for accuracy and completeness before submitting it to the appropriate review board.
7. Follow any additional instructions provided by the review board or regulatory authorities regarding the submission process.

Who needs continuing review form?

1. Researchers conducting human subjects research that requires ongoing review and oversight need to fill out the continuing review form.
2. Institutional review boards (IRBs) or ethics committees often require researchers to submit a continuing review form to ensure compliance with regulations.

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What is continuing review form?

The continuing review form is a document that researchers must submit to IRB for the review and approval of the ongoing research study.

Who is required to file continuing review form?

Researchers who are conducting an ongoing research study that has been previously approved by the IRB are required to file a continuing review form.

How to fill out continuing review form?

To fill out the continuing review form, researchers must provide updated information on the progress of the study, any changes to the study protocol, and any adverse events that have occurred.

What is the purpose of continuing review form?

The purpose of the continuing review form is to ensure that ongoing research studies remain in compliance with ethical and regulatory standards, and to determine if any modifications are needed to the study protocol.

What information must be reported on continuing review form?

Researchers must report on the progress of the study, any changes to the study protocol, any adverse events, and any other relevant information that may impact the safety and well-being of research participants.