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NAME: Human Subjects Protection Review Committee Project Description Quantitative I. Purpose: The purpose of my study is to see internet addiction in college students. a. Participants number and description:
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How to fill out human subjects protection review

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How to fill out human subjects protection review

01
To fill out the human subjects protection review, follow these steps:
02
Begin by familiarizing yourself with the guidelines and regulations for human subjects protection. This may include reading the Institutional Review Board (IRB) policies and procedures.
03
Identify the type of research study you are conducting and determine the level of review required. Some studies may be exempt from IRB review, while others require full board review.
04
Prepare all the necessary documentation and forms for submission. This may include the research protocol, informed consent forms, data collection instruments, and any other relevant materials.
05
Complete all sections of the IRB application form accurately and thoroughly. Provide detailed information about the research objectives, study design, participant selection criteria, potential risks and benefits, and any confidentiality measures in place.
06
Ensure that all investigators involved in the study have completed relevant human subjects protection training or certification.
07
Submit the completed application and all supporting materials to the appropriate IRB office for review. Follow any specific submission instructions or deadlines provided by the IRB.
08
Await feedback and approval from the IRB. They may request additional information or revisions before granting approval. Make any necessary changes and resubmit the revised materials.
09
Once the study is approved, make sure to adhere to the approved protocol and any conditions or restrictions set by the IRB.
10
If any changes need to be made to the study after approval, obtain IRB approval for the modifications before implementing them.
11
Finally, keep records of all IRB approvals, correspondence, and study-related documents for future reference and audit purposes.

Who needs human subjects protection review?

01
Various individuals and institutions may need to undergo human subjects protection review, including:
02
- Researchers and scientists conducting studies involving human participants.
03
- Universities, colleges, and other educational institutions engaged in human subjects research.
04
- Medical institutions and healthcare organizations conducting clinical trials or observational studies.
05
- Pharmaceutical companies and biomedical research facilities.
06
- Non-profit organizations and government agencies conducting social or behavioral research on human subjects.
07
It is important to determine whether your research involves human subjects and if it requires IRB review to ensure ethical and legal compliance.

What is Human Subjects Protection Review Form?

The Human Subjects Protection Review is a fillable form in MS Word extension needed to be submitted to the relevant address to provide some information. It has to be filled-out and signed, which can be done manually, or with a particular software such as PDFfiller. This tool lets you fill out any PDF or Word document right in the web, customize it depending on your requirements and put a legally-binding e-signature. Right after completion, you can easily send the Human Subjects Protection Review to the appropriate recipient, or multiple recipients via email or fax. The blank is printable too from PDFfiller feature and options presented for printing out adjustment. In both digital and in hard copy, your form should have a organized and professional look. Also you can turn it into a template to use later, without creating a new file over and over. You need just to customize the ready document.

Instructions for the Human Subjects Protection Review form

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The human subjects protection review is a process that evaluates research studies involving human participants to ensure their rights, safety, and well-being are protected.
Researchers conducting studies involving human participants are required to file a human subjects protection review.
To fill out a human subjects protection review, researchers must provide detailed information about the study protocol, risks, benefits, and procedures involving human participants.
The purpose of human subjects protection review is to ensure that research involving human participants is conducted ethically and in compliance with regulatory standards.
Researchers must report details about the study design, risks to participants, informed consent process, and measures in place to protect participants' confidentiality.
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