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Informed Consent Breast Lift (Mastery)2020 American Society of Plastic Surgeons. Purchasers of the Informed Consent Resource are given a limited license to modify documents contained herein and reproduce
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01
Read and understand the informed consent form thoroughly before filling out any information.
02
Provide accurate and honest information about your personal details and medical history.
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Seek clarification from the healthcare provider or research team if you have any questions or concerns.
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Sign and date the form only after you have fully understood and agreed to the terms and conditions.
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Keep a copy of the signed informed consent form for your records.

Who needs simplified informed consent resources?

01
Patients participating in clinical trials or research studies.
02
Individuals undergoing medical procedures or treatments.
03
Legal guardians or caregivers making medical decisions on behalf of someone else.
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Simplified informed consent resources are resources that streamline the process of obtaining informed consent from study participants in research studies.
Researchers conducting clinical trials or studies that involve human subjects are required to file simplified informed consent resources.
Simplified informed consent resources can be filled out by following the provided template and guidelines, ensuring all necessary information is included.
The purpose of simplified informed consent resources is to ensure that study participants fully understand the nature of the research study, risks involved, and their rights as participants.
Simplified informed consent resources must include information on the study objectives, procedures, potential risks and benefits, confidentiality, compensation for participation, and contact information for questions.
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