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PI Name ___ IRB #___Staff contact name ___Welcome to the Zuckerman MR Platform! Before you can schedule a scan, the following steps must be completed: You have completed the ZI MRI study application
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How to fill out citi irb flashcards

01
Gather all necessary documents and materials for your research study.
02
Log in to the CITI Program website and navigate to the IRB course module.
03
Review the course content thoroughly to understand the required information for each flashcard.
04
For each flashcard, write a clear and concise question that pertains to key concepts from the material.
05
On the reverse side of the flashcard, write a detailed answer or explanation relevant to the question.
06
Use bullet points or numbered lists for answers when applicable to enhance clarity.
07
Review and revise the flashcards to ensure accuracy and completeness before use.
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Test yourself with the flashcards regularly to reinforce learning.

Who needs citi irb flashcards?

01
Researchers preparing to submit projects for IRB approval.
02
Students enrolled in research-related courses who require ethics training.
03
Professionals involved in clinical trials or studies that demand ethical oversight.
04
Anyone looking to gain foundational knowledge on human subjects protection and research ethics.
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CITI IRB flashcards are quick reference cards used in the CITI Program to provide essential information regarding institutional review boards (IRBs) and human subject protection in research.
Researchers and institutions involved in studies that involve human subjects are required to file CITI IRB flashcards for compliance with ethical standards.
To fill out CITI IRB flashcards, one should gather required information about the research study, including the research title, principal investigator, study purpose, and methods, and then complete the designated template provided by the CITI Program.
The purpose of CITI IRB flashcards is to streamline the process of reporting human subject research activities to IRBs and ensure compliance with ethical standards and regulations.
Information that must be reported includes the title of the study, names of key personnel, a brief description of the research, participant information, and any potential risks involved.
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