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11/15/2021(A)PROTOCOL DESCRIPTION: 1. Introduction: Introduce the topic of your research with background information and citations. 2. Purpose: Clearly state what your study seeks to address and why
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01
Gather all necessary information such as organization name, date, reference number, etc.
02
Fill out the introduction section with a brief description of the purpose of the protocol.
03
Provide detailed information on the research methodology in the methods section.
04
Include any applicable regulations or ethical considerations in the compliance section.
05
Fill out the conclusion section with a summary of the findings and any recommendations for future research.
06
Review and revise the completed template for accuracy and completeness.

Who needs protocol template - university?

01
University researchers who are conducting studies that require formal documentation and approval.
02
Administrative staff who are responsible for overseeing research projects and ensuring compliance with university policies.
03
Funding agencies or sponsors who require a detailed protocol as part of the research proposal.
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The protocol template for universities is a structured document used to outline the procedures, guidelines, and regulations that researchers must follow when conducting experiments or studies involving human subjects or animals.
All researchers, faculty, and students conducting research that involves human or animal subjects are required to file the protocol template at the university.
To fill out the protocol template, researchers should provide detailed information about their study, including objectives, methodology, participant recruitment, data collection procedures, and ethical considerations. Each section must be completed as per the guidelines provided by the university.
The purpose of the protocol template is to ensure that all research projects comply with ethical standards, protect the rights and welfare of participants, and facilitate review by the university's Institutional Review Board (IRB) or animal care committee.
Information required on the protocol template includes the research title, principal investigator details, study objectives, methods, participant information, risks and benefits, informed consent process, and any funding sources.
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