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Dissent Orthodontics Supplemental Informed Consent & Questionnaire
Communicable Diseases and Your Orthodontist
(Official American Association of Orthodontics COVID-19 Consent Form)
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What is informed consent documents?
Informed consent documents are legal documents that provide participants with information about a study, including its purpose, risks, and benefits. They ensure that individuals understand what their participation entails and voluntarily agree to partake.
Who is required to file informed consent documents?
Researchers and institutions conducting studies involving human subjects are required to file informed consent documents to ensure compliance with ethical standards and regulations.
How to fill out informed consent documents?
Filling out informed consent documents involves clearly presenting the study's information, obtaining participant signatures, and ensuring that all aspects of the study are understood by the participant. It should be free of jargon and written in plain language.
What is the purpose of informed consent documents?
The purpose of informed consent documents is to protect participant autonomy by ensuring that they are fully informed about the study and to maintain ethical standards in research involving human subjects.
What information must be reported on informed consent documents?
Informed consent documents must report information about the study's purpose, procedures, risks, benefits, confidentiality, and participants' rights, including their right to withdraw at any time.
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