Get Final Report Form - Navrongo Health Research Centre :: Nhrc - Navrongo-hrc

Completing the Final Report Form for the Navrongo Health Research Centre is an essential step in the research submission process. This guide provides a clear and supportive overview to assist users in accurately filling out the form online.

Follow the steps to successfully complete your final report form.

1. Click ‘Get Form’ button to obtain the form and open it in the editor. This action allows users to access the electronic version of the report form.
2. Begin by entering the project title in the designated field. Ensure that the title precisely reflects the essence of your research project.
3. Input your IRB approval number as assigned during the initial review process. This ensures that your report is correctly linked to the original approval.
4. Specify the proposed end date of your study. This date indicates when the research activities are expected to conclude.
5. Enter the name of the principal investigator in the respective section. This person is primarily responsible for overseeing the research.
6. Provide the contact address of the principal investigator to facilitate communication regarding the final report.
7. If applicable, list any co-investigators involved in the project. Include their names and roles to give a full picture of the research team.
8. Indicate the collaborating institution if there are any partners in the research effort. This adds credibility and context to the study.
9. Enter the number of subjects studied or recruited for the project. This statistic is crucial for understanding the scope of your research.
10. Answer the question regarding whether any participants have withdrawn from the study. This is important for maintaining ethical standards.
11. Identify if any participants have been withdrawn by the research team. Documenting withdrawals is key for transparency.
12. Report on any adverse events that occurred during the study. This information is vital for assessing the safety and ethical considerations of the research.
13. Confirm whether these adverse events were reported to the IRB. This ensures that regulatory guidelines have been followed.
14. Indicate if there were any changes made to the original protocol during the research. Updates are important for regulatory compliance.
15. Document whether these changes were reported to the IRB. This maintains open communication with oversight bodies.
16. Provide details on any significant findings related to the study. Highlight what was discovered or learned through the research.
17. Complete the section on any additions or deletions to the list of investigators. This ensures the integrity of the research team.
18. State any new developments that could affect the risk/benefit ratio of the study. This is crucial for ongoing ethical review.
19. Fill in your name, contact address, email, and phone number in order to keep contact lines open.
20. Sign and date the form to validate the completion of the report. Ensure all signatures are legible to avoid any processing issues.
21. After reviewing all entries, save changes to the document. You may choose to download, print, or share the final report form as needed.

Complete your documents online to ensure a smooth submission process.