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Human and In Vitro Project Application Form Revised March 2021 3T Magnetic Resonance Research Laboratory, Diagnostic Imaging Sciences Center (DISC) AA048 UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE
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01
Identify the purpose of the study - decide whether to use human or in vitro models based on research goals.
02
Select appropriate parameters - determine relevant biological markers and conditions needed for the study.
03
For human studies, obtain ethical approval and recruit participants while ensuring informed consent.
04
For in vitro studies, choose the right cell lines that correspond to the research focus.
05
Prepare experimental setups - for human studies, design questionnaires or clinical trials; for in vitro, prepare cell cultures and necessary materials.
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Collect data systematically - ensure accuracy and consistency in data collection for both human and in vitro experiments.
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Analyze results - compare and contrast findings from both types of studies and draw conclusions.

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Human and in vitro refers to biological studies or experiments conducted on human subjects or using human cells and tissues grown outside of their natural environment (in vitro), such as in a dish or laboratory setting.
Researchers, institutions, and organizations conducting studies involving human subjects or in vitro experiments are typically required to file human and in vitro documentation as part of compliance with ethical and regulatory standards.
Filling out human and in vitro forms generally involves providing detailed information about the study design, objectives, methodologies, participant consent, and potential risks. Specific guidelines may vary depending on the regulatory body or institution.
The purpose of human and in vitro studies is to advance scientific knowledge, improve medical treatments, ensure safety and efficacy of products, and understand biological processes in a controlled manner.
Reported information typically includes study objectives, methodology, subject demographics, consent protocols, risk assessments, data collection methods, and any adverse events encountered during the study.
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