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PROTOCOL DEVELOPMENT REQUEST From Any research involving human participants, including secondary data, and human biological materials that is conducted by a faculty member, employee, student of Simon
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How to fill out protocol development request form

01
Start by downloading the protocol development request form from the official website.
02
Fill out the basic information section including your name, contact details, and project title.
03
Specify the purpose of the protocol development and provide a brief description of the project.
04
List any specific requirements or specifications for the protocol.
05
Indicate the desired timeline for the protocol development.
06
If applicable, provide any additional supporting documents or references.
07
Review the completed form for any errors or missing information.
08
Submit the form either in person or via email to the designated department or person responsible for protocol development.
09
Wait for confirmation or further instructions regarding the status of your request.

Who needs protocol development request form?

01
Anyone who requires the development of a protocol for a project or research study can use the protocol development request form. This may include researchers, scientists, students, or professionals from various fields such as medicine, engineering, social sciences, etc.
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The protocol development request form is a document used to request the development of a new protocol.
Anyone who wants to propose a new protocol or make changes to an existing protocol is required to file the protocol development request form.
To fill out the protocol development request form, you need to provide detailed information about the proposed protocol, including its purpose, objectives, methodology, and any potential risks or benefits.
The purpose of the protocol development request form is to ensure that proper review and approval processes are followed for the development of new protocols.
The protocol development request form must include information such as the protocol title, investigator's name, institution, study design, target population, and potential conflicts of interest.
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