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Human Research Protection Program Training Shana Stolarczyk, M. Ed., CIP Education and Training Coordinator, RPP Shana. Stolarczyk UCSF.edu 4155025816 www.research.ucsf.edu/chr October 19, 2015, Preparing
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Individuals participating in research or clinical studies often need to provide consent or assent. This includes both adult participants who are able to give informed consent and minors who need parental or guardian consent along with their own assent.
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Patients undergoing medical procedures, treatments, or surgeries may need to give their consent before these interventions can be performed.
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Legal contracts, such as those related to business agreements or property transactions, may require all involved parties to provide their consent and assent.
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Consent and assent may also be necessary when granting permission for the use of personal information, images, or testimonials in marketing or promotional materials.
It is important to note that the specific requirements for preparing consent and assent may vary depending on the purpose, jurisdiction, and nature of the situation. It is advisable to consult with legal professionals or authorities for guidance tailored to your specific needs.
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Preparing consent and assent involves obtaining permission from individuals before conducting certain activities or procedures.
Researchers, medical professionals, and organizations working with human subjects are required to file preparing consent and assent.
Preparing consent and assent forms typically involve providing clear information about the study or procedure, risks and benefits, confidentiality, and obtaining signatures from participants.
The purpose of preparing consent and assent is to ensure that individuals understand the nature of the study or procedure, potential risks involved, and voluntarily agree to participate.
Preparing consent and assent forms must include information about the study or procedure, risks and benefits, confidentiality measures, contact information for questions, and participant signatures.
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