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Community Hospital of the Monterey Peninsula Institutional Review Boarded PROTOCOL APPLICATIONINITIAL REVIEWProtocol Number and Full Title: Research sponsor: 1. Type of funding:Industry Foundation
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How to fill out new protocol application template

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How to fill out new protocol application

01
Start by opening the new protocol application form.
02
Read the instructions provided in the form to understand the requirements.
03
Fill out the basic information section, including the project title, principal investigator's name, and contact details.
04
Provide a clear and concise description of the project objectives and the research methodology.
05
Specify any ethical considerations or potential risks associated with the project.
06
Include details about the target population or sample size, if applicable.
07
Attach any supporting documents or additional information required.
08
Review the completed application for any errors or missing information.
09
Submit the filled-out new protocol application form to the designated authority.
10
Await approval and follow any further instructions communicated by the authority.

Who needs new protocol application?

01
Researchers who are planning to conduct a research project that involves human subjects or/and animals, typically need to fill out a new protocol application. Additionally, students, scientists, or professionals involved in experimental studies or clinical trials may also require a new protocol application.

What is NEW PROTOCOL APPLICATION Form?

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New protocol application is a form used to submit a request for approval to conduct research involving human subjects.
Researchers conducting studies involving human subjects are required to file a new protocol application.
The new protocol application should be filled out accurately and completely with all relevant information about the study.
The purpose of a new protocol application is to ensure that research involving human subjects is conducted ethically and in accordance with regulations.
Information such as study objectives, methodology, risks to participants, and informed consent procedures must be reported on the new protocol application.
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