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How to Sign Acupuncture Medical Consent

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new videos every day Im Janice Lee Im a licensed acupuncturist with a Texas State Board of Medical Examiners and we have Amy here who is going to receive acupuncture for the first time and I have assured her that theres nothing to be afraid of that it doesnt hurt and that acupuncture is only one way that we can access the human Meridian system so I think that Amys ready we have followed clean needle technique protocols and swab the area Im going to use a five needle protocol that was designed by a French doctor that Ive worked with for several years through Palpa Tory diagnosis which would be the feeling of the radial pulse and feeling at different depths in areas for different qualities in the pulse on both sides is the main form of palpite or a diagnosis that we use in oriental medicine now keep in mind that in oriental medicine it evolved for thousands of years without the ability to see inside the body in other ways like we have today with all the medical imaging devices t

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Below are some common questions from our customers that may provide you with the answer you're looking for. If you can't find an answer to your question, please don't hesitate to reach out to us.

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Whose responsibility is it to obtain an informed consent?

THE DUTY TO OBTAIN INFORMED CONSENT The duty to obtain a patients consent for treatment rests on the patients treating physician (6). Hospitals, nurses, surgical assistants, and referring physicians do not owe this duty to their patients (7).

Should I sign the consent form?

Why do I have to sign a consent form? The main purpose of the informed consent process is to protect the patient. A consent form is a legal document that ensures an ongoing communication process between you and your health care provider.

Is the person signing the consent forms the patient?

Date and time the informed consent form is signed by the patient or the patients legal representative.

Who can witness the signing of informed consent?

Any member of the healthcare team may sign as a witness to the patients signature, although this serves only to verify that it was the patient who signed the form.

Does informed consent need to be signed?

The subject or the subjects legally authorized representative must sign and date the short form. The witness must sign both the short form and a copy of the summary, and the person actually obtaining the consent must sign a copy of the summary.

How do I write an informed consent form?

The informed consent document should succinctly describe the research as it has been presented in the IRB application. Use the second (you) or third person (he/she) to present the study details. Avoid use of the first person (I). Include a statement of agreement at the conclusion of the informed consent document.

Who signs the informed consent form?

The subject or the subjects legally authorized representative or the parent(s) must sign the short form, and the person actually obtaining the consent must sign the copy of the summary (45 CFR 46.117(b)(2)).

Does the doctor need to sign the informed consent?

Additionally, the consent document must be signed and dated by the patient (or the patients legal guardian or representative). Many consent forms also require a healthcare provider signature. Consent forms should include statements to be signed by the patient and the healthcare provider.

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