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Get the free Informed Consent Process - URSA - Georgia State University

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Georgia State University Department of AthleticsAssumption of Risk, Waiver of Liability & Indemnity Agreement Sports Arena Basketball Courts Participant Information University Status: Faculty Staff
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How to fill out informed consent process

01
Start by clearly explaining the purpose and nature of the study or procedure to the participant.
02
Provide relevant information regarding the risks, benefits, and alternatives to the proposed intervention.
03
Make sure to use simple and clear language, avoiding technical jargon as much as possible.
04
Answer any questions or concerns the participant may have, ensuring their understanding of the information provided.
05
Allow sufficient time for the participant to carefully review the consent form and ask additional questions.
06
Ensure that the participant is fully aware of their voluntary participation and their right to withdraw at any time.
07
Document the consent process by having the participant sign the informed consent form, or by any other means of legally accepting their agreement.
08
Provide a copy of the signed consent form to the participant for their records.
09
Continuously monitor and ensure ongoing informed consent throughout the duration of the study or procedure, as new information may arise.

Who needs informed consent process?

01
Any individual who is participating in a research study or undergoing a medical procedure that involves potential risks, benefits, or alternatives.
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The informed consent process is a procedure to ensure that individuals are fully aware of the risks and benefits of participating in a research study or medical treatment before agreeing to take part.
Researchers, healthcare providers, or medical professionals conducting a study or providing treatment are required to file the informed consent process.
The informed consent process is typically filled out by providing detailed information about the study or treatment, discussing the risks and benefits with the individual, and obtaining their signature to indicate their understanding and agreement.
The purpose of the informed consent process is to protect the rights and welfare of individuals by ensuring they understand the risks and benefits of their participation in a study or treatment.
The informed consent process must include information about the study or treatment, potential risks and benefits, voluntary participation, confidentiality, and contact information for questions.
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