Get the free SRC Protocol Review Form - OU Medicine

THE OF CANCER INSTITUTE SCIENTIFIC REVIEW COMMITTEE STANDING OPERATING PROCEDURE Revised 12/01/2009 TABLE OF CONTENTS Function of Scientific Review Committee 3 Membership 3 Protocol Definitions 5

How to fill out src protocol review form

Who needs src protocol review form?

1. Any researcher or scientist conducting a study involving human subjects may need to fill out an src protocol review form. This includes individuals working in academic institutions, pharmaceutical companies, or clinical settings.
2. Institutional Review Boards (IRBs) or ethics committees often require researchers to submit an src protocol review form before beginning their study. These review boards ensure the rights and welfare of the participants are protected and that the study meets ethical standards.

How to fill out src protocol review form:

1. Start by carefully reading the instructions and guidelines provided with the src protocol review form. Familiarize yourself with the required information and any specific formatting or documentation requirements.
2. Begin by providing general information about the study, such as the title, principal investigator's name, department or institution, and contact information. Make sure to include any co-investigators or collaborators involved in the study.
3. Clearly state the objectives and purpose of the study. Explain why the research is important, how it will contribute to existing knowledge, and the potential benefits for participants or society.
4. Describe the study design and methodology in detail. Include information about the research design, sample size, recruitment strategies, data collection methods, and any interventions or treatments involved. Be sure to address potential risks or adverse effects and how they will be managed.
5. Outline the inclusion and exclusion criteria for participants. Specify the characteristics or demographics of individuals who will be eligible or ineligible to participate in the study.
6. Provide a comprehensive plan for obtaining informed consent from participants. Describe how participants will be fully informed about the study's purpose, procedures, potential risks, benefits, and their rights as research subjects. Include a consent form template that participants will sign.
7. Address the ethical considerations and safeguards in place to protect participants. Discuss measures to ensure confidentiality, privacy, and data handling. Explain how participants' autonomy and well-being will be respected throughout the study.
8. Detail the plan for data analysis and dissemination of results. Explain how the data will be collected, managed, analyzed, and reported. If applicable, outline any plans for publishing or sharing the findings with the scientific community or the public.
9. Attach any supporting documents required, such as study protocols, questionnaires, consent forms, recruitment materials, or any relevant literature or references.
10. Review the completed src protocol review form for accuracy and completeness. Ensure that all sections are filled out correctly and that all necessary information and signatures are provided. Make a copy for your records and submit the form to the appropriate ethics committee or IRB.

Remember to check with your institution or ethics committee for any specific requirements or modifications to the src protocol review form. It is important to adhere to all guidelines and regulations to ensure the ethical conduct of research involving human subjects.

For pdfFiller’s FAQs

What is src protocol review form?

The src protocol review form is a document used to evaluate and assess the proposed research involving human subjects, animals, or biohazardous materials.

Who is required to file src protocol review form?

Researchers and institutions conducting research that involves human subjects, animals, or biohazardous materials are required to file the src protocol review form.

How to fill out src protocol review form?

To fill out the src protocol review form, you need to provide detailed information about the research project, including its objective, methodology, potential risks, and the mitigation measures put in place.

What is the purpose of src protocol review form?

The purpose of the src protocol review form is to ensure that research involving human subjects, animals, or biohazardous materials is conducted ethically and in compliance with regulatory standards.

What information must be reported on src protocol review form?

The src protocol review form typically requires information on the research project's objectives, study design, participant selection criteria, proposed procedures, potential risks to participants, and plans for informed consent and data management.

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