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Annex 1 Form AF/01010/2020/01.4PROTOCOL SUBMISSION FORM FOR CLINICAL Rialto be filled by Principal Investigator (copy of 2)Please fill out the form completely and return to the Secretariat of MAIN
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How to fill out new protocol submission form

01
Start by entering the required information in the designated fields such as title, researcher name, and affiliation.
02
Provide a brief summary of the research objective and the hypothesis being tested in the appropriate section.
03
Specify the study design, methodology, and data collection procedures.
04
Clearly state the inclusion and exclusion criteria for the participants in the study.
05
Describe the ethical considerations and steps taken to ensure participant consent and data protection.
06
Outline the expected outcomes and potential impact of the research.
07
Provide a detailed plan for data analysis and statistical methods to be employed.
08
Include any supporting documents or references that are relevant to the research proposal.
09
Review the completed form for accuracy and completeness before submission.
10
Submit the filled-out new protocol submission form through the designated platform or to the specified authority.

Who needs new protocol submission form?

01
Researchers and scientists who wish to propose a new research protocol or study

What is New Protocol Submission - Nova Southeastern University Form?

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The new protocol submission form is a document required for submitting a research or clinical trial protocol to an oversight body for review and approval.
Researchers, principal investigators, or institutions conducting studies involving human subjects or animals are typically required to file the new protocol submission form.
To fill out the new protocol submission form, provide detailed information about the study's objectives, methodology, participant criteria, risks, benefits, and any other required sections as indicated by the oversight body.
The purpose of the new protocol submission form is to ensure that the proposed research adheres to ethical standards, safeguards participant welfare, and complies with applicable regulations.
The form typically requires information such as study title, investigator details, study objectives, participant eligibility criteria, study design, methodology, statistical analysis plan, and potential risks and benefits.
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