Get the free Continuing Review Form - navrongo-hrc

SARONG HEALTH RESEARCH Center INSTITUTIONAL REVIEW BOARD P. O BOX 114 SARONG U/E REGION, GHANA IRB×sarong.sitcom.org Tel: (233) (0)3821 22348, Fax: (233) (0)3821 22320 CONTINUING REVIEW SUBMISSION

How to fill out continuing review form

How to fill out a continuing review form:

1. Start by carefully reading the instructions provided on the form. Make sure you understand the purpose of this review and any specific requirements.
2. Gather all the necessary information and documentation required to complete the form. This may include previous study protocols, consent forms, adverse event reports, and any other relevant materials.
3. Begin by providing basic information about the research study, such as the study title, researcher's name, contact information, and any identifying numbers or codes associated with the study.
4. Next, answer any questions regarding the progress of the study. This may include information about recruitment, enrollment numbers, current status of participants, and any changes made to the study design or procedures since the last review.
5. Evaluate the risk and benefit aspects of the research. Some questions on the form may inquire about the potential harm to participants, how risks are being minimized, and how benefits have been demonstrated or can be expected.
6. Describe any adverse events that have occurred since the last review. Include details about the event, its impact on participants, any actions taken, and any changes in the study as a result.
7. Assess the consent process and any changes made to it. Discuss how informed consent is obtained, whether it is ongoing, and any modifications made to the consent form or process.
8. Provide information about any amendments or modifications made to the study protocol since the last review. Explain the reasons for these changes and their potential impact on participant safety or study outcomes.
9. Discuss any data or interim analyses conducted during the study as well as their implications. Share any significant findings, data integrity issues, or changes made as a result of the analyses.
10. Finally, make sure to sign and date the form once you have completed all the necessary sections. Attach any supporting documents or materials as required.

Who needs a continuing review form?

1. Researchers involved in human subjects research need to complete a continuing review form. This form is usually required when conducting studies that involve human participants to ensure that the ongoing research is ethical, safe, and adheres to any regulations or guidelines.
2. Institutional Review Boards (IRBs) or Ethics Committees overseeing the research study also need the continuing review form. They use the information provided in the form to assess the progress of the study, review any changes, and make decisions regarding the ongoing approval of the research.
3. Regulatory bodies or funding organizations may also require the submission of continuing review forms as part of their oversight responsibilities. This helps ensure compliance with regulations, guidelines, and ethical standards.

In summary, a continuing review form must be filled out by researchers involved in human subjects research to assess the progress, safety, and ethical considerations of their study. This information is used by IRBs, ethics committees, and regulatory bodies to make decisions regarding the ongoing approval of the research.

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What is continuing review form?

Continuing review form is a document used to assess the progress of an ongoing research study and ensure that it continues to meet ethical and regulatory standards.

Who is required to file continuing review form?

Researchers and their institutions are required to file a continuing review form for research studies that involve human subjects.

How to fill out continuing review form?

Continuing review forms are typically completed online through the institution's research compliance system. Researchers must provide updates on study progress, any adverse events, and any modifications to the research protocol.

What is the purpose of continuing review form?

The purpose of the continuing review form is to ensure that research studies involving human subjects are being conducted ethically and in accordance with regulations.

What information must be reported on continuing review form?

Researchers must report any changes to the study protocol, adverse events, and progress updates on the continuing review form.