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Version Date: 10/31/17Protocol No. HCI IRB # 105517 A Phase II Trial Assessing the Accuracy of Tumor Bed Biopsies in Predicting Pathologic Response in Patients with Clinical/Radiologic Complete Response
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To fill out protocol no hci irb, follow these steps:
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Begin by providing the title of the protocol.
03
Clearly state the purpose of the protocol.
04
Include a detailed description of the study design and methodology to be used.
05
Specify the target population and the sample size.
06
Clearly define the inclusion and exclusion criteria for participants.
07
Describe the data collection procedures and instruments to be used.
08
Explain any potential risks and benefits associated with the study.
09
Outline the data analysis plan to be used.
10
Provide a timetable for the completion of the study.
11
Include any necessary informed consent forms or other required documentation.
12
Review and revise the protocol as needed before submission to the HCI IRB.
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Protocol no hci irb is needed by researchers or individuals conducting studies or experiments that involve human participants. It is a requirement to ensure ethical considerations and protection of human subjects in research.
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What is protocol no hci irb?
Protocol no hci irb is a specific protocol related to human subject research conducted at the institution.
Who is required to file protocol no hci irb?
Researchers and institutions conducting human subject research are required to file protocol no hci irb.
How to fill out protocol no hci irb?
Protocol no hci irb can be filled out by providing detailed information about the research project, participants, potential risks, and safety measures.
What is the purpose of protocol no hci irb?
The purpose of protocol no hci irb is to ensure that human subject research is conducted ethically and with the safety and well-being of participants in mind.
What information must be reported on protocol no hci irb?
Information such as study aims, methodology, participant recruitment, informed consent process, risks and benefits, and confidentiality measures must be reported on protocol no hci irb.
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