Get the free IRB CONTINUING STUDY APPLICATION FORM 120117 - machias

Institutional Review Board Continuing Study Application Form Protocol # Study Title: Name of Applicant:1 Principal Investigator:2 Address: Address: Email: Email: Telephone: Telephone: 1 Primary contact

How to fill out irb continuing study application

How to fill out IRB continuing study application:

1. Start by reviewing the instructions provided by your institution's IRB. These instructions will provide you with important information and guidelines for completing the application.
2. Gather all the necessary documents and information required for the application. This may include a detailed description of the study, consent forms, recruitment materials, survey questionnaires, and any other supporting documents.
3. Begin filling out the application form by providing basic information about the study, such as the title, principal investigator's name, and contact details.
4. Follow the instructions and provide detailed information about the study design, methods, and procedures. This may involve explaining the research objectives, data collection methods, interventions, and any potential risks or benefits involved.
5. In the application form, clearly state the inclusion and exclusion criteria for participants, as well as the recruitment strategies that will be utilized.
6. Describe the informed consent process and provide a copy of the consent form(s) for the participants to review and sign. Include information on how participants will be informed about the study and how their privacy and confidentiality will be protected.
7. Discuss the potential risks and benefits of the study and how you plan to mitigate any risks to participants. If necessary, provide documentation of the necessary approvals (e.g., FDA approvals for investigational drugs or devices).
8. Explain how you will ensure the data integrity, storage, and protection of participant information. Provide details on data handling procedures, including how long the data will be retained and how it will be disposed of after the study is completed.
9. Answer any additional questions or sections specified in the application form, such as details on conflicts of interest, financial disclosures, and any changes that have occurred since the initial approval of the study.
10. Once you have completed the application, double-check all the information for accuracy and completeness. Make sure to sign and date the application form before submitting it to the IRB for review.

Who needs IRB continuing study application?

1. Researchers who are conducting studies that involve human subjects and have previously obtained initial IRB approval for their project.
2. Researchers who need to make changes or amendments to their approved study, including modifications to the study design, recruitment procedures, consent forms, or any other aspect of the research.
3. Researchers who have completed their initial study and wish to continue collecting data or follow-up with study participants for additional analysis or evaluation.

Note: It is essential to consult your institution's IRB guidelines and policies and seek guidance from your IRB office for specific requirements and instructions related to the IRB continuing study application.

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What is irb continuing study application?

The IRB continuing study application is a form that researchers must submit to continue their approved research involving human subjects.

Who is required to file irb continuing study application?

Researchers who have been approved to conduct research involving human subjects are required to file an IRB continuing study application.

How to fill out irb continuing study application?

Researchers must provide updated information on their research progress, any changes to the study protocol, and any adverse events that may have occurred during the study period.

What is the purpose of irb continuing study application?

The purpose of the IRB continuing study application is to ensure that research involving human subjects continues to meet ethical guidelines and regulations.

What information must be reported on irb continuing study application?

Researchers must report on their research progress, any changes to the study protocol, and any adverse events that may have occurred during the study period.