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Advisory and Informed Consent to Treatment i. Patient Advisory to Consult a Physician In keeping with Article 160, Section 821 1.1 ×b) of NYS Education law, we are asked that you sign below in order

How to fill out advisory and informed consent

How to fill out advisory and informed consent:

1. Begin by reviewing the advisory and informed consent form thoroughly to understand its purpose and the information that needs to be provided.
2. Fill out the required personal information accurately, including your name, contact details, date of birth, and any other required demographics.
3. Read through each section carefully and make sure you understand the nature of the research or procedure being conducted. Seek clarification from the investigator or healthcare professional if needed.
4. Acknowledge your understanding of the risks and benefits associated with the research or procedure by signing and dating the appropriate sections.
5. Address any questions or concerns you may have with the investigator or healthcare professional before signing the form. It is essential to ensure that you have a clear understanding of what you are consenting to.
6. After reading and reviewing the form thoroughly, sign and date it in the designated areas to indicate your informed consent.
7. If applicable, consider having a witness also sign and date the form to provide additional authentication of your consent.

Who needs advisory and informed consent:

1. Individuals participating in research studies: Advisory and informed consent is required for individuals volunteering to participate in research studies to ensure that they fully understand the purpose, procedures, risks, and benefits associated with the study.
2. Patients undergoing medical or surgical procedures: Informed consent is necessary for patients undergoing medical or surgical procedures, ensuring they are fully informed about the nature of the procedure, potential risks, alternatives, and expected outcomes.
3. Individuals receiving experimental treatments: Advisory and informed consent is essential for individuals who are receiving experimental treatments or participating in clinical trials. This allows them to make an informed decision about whether to proceed with the treatment, considering the potential risks and benefits.

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