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Suzhou Kin tor Pharmaceuticals, Inc. Model Informed Consent FormGT0918US3001, Version 2.0, 09 July 2021CONFIDENTIALMODEL INFORMED CONSENT FORM VERSION LOG VersionDateReason for Change1.013 April 2021Not
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01
Review the entire informed consent form to understand what information needs to be provided.
02
Fill in the required personal information such as name, age, address, etc.
03
Sign and date the form to indicate your agreement and understanding of the information provided.
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Attend any necessary meetings or discussions with a healthcare provider to go over the form and ask any questions.
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Keep a copy of the signed consent form for your records.

Who needs model informed consent form?

01
Individuals who are participating in a research study or clinical trial.
02
Patients undergoing medical procedures or treatments.
03
Individuals receiving counseling or therapy services.
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A model informed consent form is a standardized document used to provide individuals with information about the nature, risks, benefits, and procedures of a study or treatment so that they can make an informed decision about participation.
Researchers and organizations conducting clinical trials or studies involving human subjects are typically required to file a model informed consent form.
To fill out a model informed consent form, one must provide clear and comprehensive information about the study, including its purpose, procedures, risks, benefits, and details on confidentiality, as well as gather the participant's signature to indicate their consent.
The purpose of the model informed consent form is to ensure that participants are fully aware of and agree to the terms of participation in a study, protecting their rights and well-being.
The model informed consent form must report information such as the purpose of the study, procedures involved, potential risks and benefits, alternatives to participation, confidentiality measures, and the right to withdraw.
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