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Get the free CUMC IRB# AAAQ3153 - Version Date: 05SEP2018

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Columbia University Medical Center Herbert Irving Comprehensive Cancer Center CUMC IRB# AAAQ3153 Version Date: 05SEP2018NCT02716038CUMC IRB#: AAAQ3153 Celgene Protocol Identifier AXCLNSCLCPI005652
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How to fill out cumc irb aaaq3153

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How to fill out cumc irb aaaq3153

01
Visit the CUMC IRB website and locate the AAQ3153 form.
02
Carefully read the instructions provided for completing the form.
03
Fill in the project title and principal investigator's details.
04
Provide a summary of the research project, including objectives and methods.
05
Describe the potential risks to participants and how they will be mitigated.
06
Include information about participant recruitment and informed consent procedures.
07
Attach any supporting documents required, such as questionnaires or consent forms.
08
Review the completed form for accuracy and completeness.
09
Submit the form electronically via the designated submission portal.

Who needs cumc irb aaaq3153?

01
Researchers planning to conduct studies involving human participants at CUMC.
02
Students conducting research requiring IRB approval for their thesis or dissertation.
03
Faculty members submitting grant applications that involve human subjects.
04
Any staff involved in research protocols requiring ethical review and oversight.
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cumc irb aaaq3153 refers to a specific form or document related to the Institutional Review Board (IRB) at Columbia University Medical Center (CUMC), typically used for research protocol submissions or compliance.
Researchers or investigators conducting studies involving human subjects at CUMC are required to file cumc irb aaaq3153.
To fill out cumc irb aaaq3153, researchers must provide detailed information about the study design, objectives, participant recruitment, informed consent processes, and any potential risks involved, following the guidelines provided by the CUMC IRB.
The purpose of cumc irb aaaq3153 is to ensure that research projects adhere to ethical standards and protect the rights and welfare of human subjects involved in research.
The information that must be reported on cumc irb aaaq3153 includes study title, principal investigator details, objectives, methods, risks, benefits, informed consent procedures, and data management plans.
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