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DRPractice Number:Address: (Hereinafter your/the Dental Professional)ACTIVE ALIGNERS INFORMED CONSENT AND AGREEMENT It is important to understand the risks and benefits of undergoing any treatment
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How to fill out informed consent form for

01
Read through the informed consent form thoroughly to understand all the terms and conditions.
02
Fill out all the necessary personal information accurately, including your name, date of birth, and contact details.
03
Sign and date the form to indicate that you have consented to participate in the activity or treatment described.
04
If there are sections requiring additional information or initials, make sure to complete those as well.
05
Keep a copy of the signed form for your records and return the original to the appropriate party.

Who needs informed consent form for?

01
Informed consent forms are typically required for participants in research studies, clinical trials, medical procedures, surgeries, and other situations where individuals need to understand and agree to the risks and benefits involved.

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Informed consent forms are used to ensure that individuals are provided with all necessary information before agreeing to participate in a research study or medical procedure.
Researchers, healthcare providers, or individuals conducting a study or performing a medical procedure are required to file informed consent forms for participants or patients.
Informed consent forms should be filled out by providing all relevant information about the study or procedure, risks and benefits, confidentiality, voluntary participation, and any other details required by the institutional review board or ethics committee.
The purpose of informed consent forms is to ensure that individuals understand the risks and benefits associated with their participation in a study or procedure, and to give them the opportunity to make an informed decision about whether or not to participate.
Informed consent forms should include information about the study or procedure, risks and benefits, confidentiality of data, voluntary participation, contact information for questions, and any other details required by the institutional review board or ethics committee.
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