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Acknowledgement of Informed Consent and Authorization acknowledge that I, the undersigned, voluntarily participate in the treatment of acupuncture at the Center for Complementary Medicine Inc. I am
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01
Begin by reading the entire informed consent document carefully.
02
Make sure you understand all the information provided in the document.
03
Fill in your personal details in the designated spaces such as your name, address, age, etc.
04
Review the study or procedure description thoroughly to ensure you are aware of what you are consenting to.
05
Pay attention to any risks, benefits, or alternative treatments mentioned in the document.
06
If you have any questions or concerns, it is best to clarify them with the research team or healthcare provider before signing.
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If you are satisfied with the information and wish to provide consent, sign and date the acknowledgement of informed consent form.
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Make sure to keep a copy of the signed document for your records.

Who needs acknowledgement of informed consent?

01
Anyone participating in medical research studies, clinical trials, or medical procedures that require informed consent.
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Acknowledgement of informed consent is a document that confirms that a participant has been adequately informed about a study or procedure, understands the details, and voluntarily agrees to take part in it.
Researchers, healthcare providers, or institutions conducting studies or medical procedures that involve human participants are required to file acknowledgement of informed consent.
To fill out an acknowledgement of informed consent, the researcher or provider must provide clear information about the study, including its purpose, procedures, risks, and benefits, and obtain the signature of the participant indicating their agreement.
The purpose of acknowledgement of informed consent is to ensure that participants are fully informed about what they are agreeing to, thereby protecting their rights and autonomy in research or medical procedures.
The acknowledgement of informed consent must include the study's purpose, procedures, potential risks and benefits, confidentiality measures, and contact information for questions, as well as the participant's signature and date.
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