Get Annamalai University Experiment Permission Form

The Annamalai University Experiment Permission Form is an essential document for obtaining approval to conduct experiments involving human participants. This guide will walk you through the process of filling out the form online, ensuring that you provide all necessary information accurately and effectively.

Follow the steps to complete the form with ease.

1. Click the ‘Get Form’ button to obtain the form and open it in the editor.
2. Begin filling out Part-A by stating the place where the experiment will be performed in the designated field.
3. Enter the date the experiment is set to commence and its duration. Ensure you have the appropriate research proposal (Part B) ready to append to this form.
4. Provide your name and designation as the chief investigator. Be sure to include your signature, the date, and the place of signing.
5. Complete Form-B by entering the project title in the specified area.
6. Specify the type of study, choosing from options such as drug trial, vaccine trial, surgical procedure, or others as applicable.
7. List the names, designations, and qualifications of all investigators involved. Make sure to include a medical doctor as a co-guide.
8. Detail the place where the experiment will be performed and indicate whether it falls under the jurisdiction of the Institutional Ethics Committee (IEC).
9. Outline the research objectives and provide a rationale for undertaking the investigation with human subjects.
10. Describe the recruitment procedures for subjects and the inclusion/exclusion criteria for entry into the study.
11. Provide a precise description of the methodology, including dosage, treatment duration, and any invasive procedures.
12. Elaborate on plans for informed consent, ensuring that forms are provided in relevant languages.
13. Assess the proposed interventions' safety, including any necessary laboratory reports.
14. Indicate if the study entails more than minimal risk and provide plans for managing potential risks.
15. List proposed compensation for participants and detail how data will be stored and maintained.
16. Discuss the plans for publication of results, emphasizing the privacy and confidentiality of participants.
17. Address ethical issues that may arise during the study and the steps taken to mitigate them.
18. Include relevant documents required for the study protocol, ensuring copies are attached.
19. Agree to comply with national and international Good Clinical Practice (GCP) protocols.
20. Identify funding agencies or sponsors involved in your research and detail the allocation of funds.
21. Complete the investigator’s declaration by certifying various aspects of your research proposal.
22. Review all entered information for accuracy before submitting. You can save changes, download, print, or share the form as needed.

Start completing your required documents online today!