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Informed Consent Form for NonMedical ResearchApplication number at the Ethics Committee (to be completed by the Committee secretariat): I the undersigned:Name and Surname:ID Number: Address: Zip code:a)
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How to fill out expedited ethical review process

01
Step 1: Gather all the necessary documents and information required for the expedited ethical review process.
02
Step 2: Review the guidelines and instructions provided by the ethical review committee.
03
Step 3: Prepare a clear and concise research proposal or study protocol.
04
Step 4: Complete the application form provided by the ethical review committee.
05
Step 5: Attach all the required supporting documents, such as informed consent forms and recruitment materials.
06
Step 6: Submit the application and supporting documents to the ethical review committee.
07
Step 7: Pay any applicable fees or processing charges.
08
Step 8: Wait for the ethical review committee to review and evaluate your application.
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Step 9: Address any concerns or queries raised by the committee, if applicable.
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Step 10: Await the final decision from the ethical review committee and comply with any necessary modifications or requirements.

Who needs expedited ethical review process?

01
Researchers conducting studies or experiments involving human subjects.
02
Research institutions or organizations conducting experiments or studies on human participants.
03
Pharmaceutical companies or clinical trial sponsors conducting human research.
04
Healthcare professionals conducting research that involves patient data or interventions.
05
Any individual or entity involved in research that may have ethical implications or involves human participants.

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The expedited ethical review process is a streamlined review procedure designed to evaluate research proposals that entail minimal risk to participants. It allows for a quicker approval compared to the full review process, enabling researchers to initiate their studies in a timely manner.
Researchers conducting studies involving human subjects that are classified as minimal risk are required to file for an expedited ethical review process. This typically includes faculty, students, and staff affiliated with the institution conducting the research.
To fill out the expedited ethical review process, researchers need to complete an application form that outlines their study's objectives, methodology, participant recruitment, data handling, and ethical considerations. Additional documents, such as informed consent forms, must also be submitted as part of the application.
The purpose of the expedited ethical review process is to facilitate timely reviews of research studies that pose minimal risk to participants while ensuring ethical standards are met. It aims to provide efficient oversight without compromising participant safety and ethical considerations.
Information that must be reported includes the research title, principal investigator details, study objectives, participant demographics, recruitment methods, data collection and analysis plans, potential risks and benefits, and measures to protect participant confidentiality.
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