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JSOAP2US01 Version 7.0, May 14, 2018Page 1 of 66A Phase 2, DoubleClick, Randomized, Controlled Study to Evaluate the Efficacy and Safety of Joints, Autologous Adipose Tissue Derived Mesenchymal Stem
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Institutional review boards (IRBs) also require researchers to have a protocol and informed consent as part of the study approval process.
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Protocol is a detailed plan of a scientific or medical experiment, treatment, or procedure. Informed consent is the process by which a patient or research subject is informed about and agrees to participate in a study.
Researchers, doctors, and other healthcare professionals conducting studies or medical treatments are required to file protocol and informed consent.
Protocol and informed consent forms are typically filled out by the researcher or healthcare professional conducting the study or treatment, with input from the patient or research subject.
The purpose of protocol and informed consent is to ensure that research studies and medical treatments are conducted ethically and with the full knowledge and agreement of the patient or research subject.
Protocol and informed consent forms typically require information about the study or treatment, potential risks and benefits, and the patient or research subject's rights.
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