Get the free Continuing review form - Liberty IRB

CONTINUING REVIEW FORM Special Laboratory Testing Consent 1. 2. 3. 4. 5. 6. 7. SPECIAL LABORATORY TESTING CONSENT Liberty IRB Tracking Number: Name of Document: Name of Principal Investigator: Original

How to fill out continuing review form

How to fill out continuing review form:

1. Start by carefully reviewing the instructions provided with the continuing review form. Make sure you understand the purpose and requirements of the form before proceeding.
2. Gather all the necessary information and documents that may be required to complete the form. This may include previous study protocols, participant consent forms, and any relevant study data or findings.
3. Begin filling out the form by providing the required basic information about the study, such as the title, principal investigator, and study start date. Ensure that all the information is accurate and up to date.
4. Move on to the section where you may need to provide information about any changes or updates that have occurred since the last review. This may include modifications to the study protocol, participant enrollment numbers, or adverse events that have been reported.
5. Be thorough in describing any changes or updates that have taken place, ensuring that you provide enough detail for the reviewers to understand the impact and significance of these changes.
6. If applicable, provide any supporting documentation or evidence to support the changes or updates that you have mentioned. This could include revised study protocols, updated participant consent forms, or any relevant data or analysis.
7. Complete any additional sections or questions on the form that pertain to your specific study. This may include sections on participant safety, data monitoring, or any other requirements that are relevant to your study.
8. Review the filled-out form carefully before submitting it. Make sure all the information is accurate, clear, and consistent. Double-check for any errors or omissions that may have occurred during the process.
9. Finally, submit the form according to the specified instructions and within the given timeline. Ensure that you keep a copy of the completed form for your records.

Who needs continuing review form?

1. Researchers who are conducting studies that involve human participants may need to fill out a continuing review form.
2. Institutional Review Boards (IRBs) or ethics committees responsible for overseeing research involving human participants may require researchers to submit a continuing review form.
3. Organizations or institutions that have established guidelines or regulations regarding the conduct of research involving human participants may also require the use of a continuing review form.

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What is continuing review form?

Continuing review form is a document submitted to the Institutional Review Board (IRB) to ensure that an ongoing research study is still in compliance with ethical standards and regulations.

Who is required to file continuing review form?

Researchers conducting human subjects research are required to file continuing review form.

How to fill out continuing review form?

Continuing review form can be filled out by providing updated information on the research study, any changes in protocol, and any adverse events.

What is the purpose of continuing review form?

The purpose of continuing review form is to ensure that ongoing research studies involving human subjects remain ethical and compliant with regulations.

What information must be reported on continuing review form?

Information such as any changes in protocol, adverse events, updated contact information, and any new documentation must be reported on continuing review form.