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SUPPLEMENTAL INFORMED CONSENT & HEALTH QUESTIONNAIRE Orthodontic Treatment in the Era of COVID-19 Thank you for your continued trust in our practice. As with the transmission of any communicable disease
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01
Read the supplemental informed consent form thoroughly to understand its purpose and requirements.
02
Collect all necessary information and materials, such as the participant's personal details and relevant medical history.
03
Ensure that the participant understands the risks, benefits, and potential side effects of participating in the covid-19 study.
04
Clearly explain the purpose of the supplemental informed consent form and its connection to the main consent form.
05
Provide ample opportunity for the participant to ask questions and seek clarification about any aspect of the form.
06
Ensure that the participant voluntarily signs and dates the supplemental informed consent form.
07
Keep a copy of the filled-out form for record-keeping purposes.
08
Follow any additional guidelines or instructions provided by the organization conducting the covid-19 study while filling out the form.

Who needs supplemental informed consent covid-19?

01
Participants who are considering taking part in a covid-19 study or research that requires additional consent beyond the standard consent form.
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Supplemental informed consent covid-19 is an additional agreement or document that provides further information and clarification for participants in covid-19 related studies or trials.
Researchers, investigators, or healthcare providers conducting covid-19 related studies or trials are required to file supplemental informed consent.
Supplemental informed consent covid-19 can be filled out by including additional information, risks, benefits, and any updates to the original informed consent document.
The purpose of supplemental informed consent covid-19 is to ensure participants have all the necessary information to make an informed decision regarding their participation in covid-19 related studies or trials.
Supplemental informed consent covid-19 must include any new information, updates on the study or trial, potential risks, benefits, and any changes to the original consent form.
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