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INFORMED CONSENTDental Treatment in the Era of COVID19Thank you for your continued trust in our practice. As with the transmission of anycommunicable disease like a cold or the flu, you may be exposed
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How to fill out supplemental informed consent form
How to fill out supplemental informed consent form
01
Read the supplemental informed consent form thoroughly to understand its purpose and contents.
02
Provide all necessary personal information as required in the form.
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Sign and date the form to acknowledge your understanding and agreement with its contents.
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If needed, have a witness sign the form as well.
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Keep a copy of the completed form for your records.
Who needs supplemental informed consent form?
01
Individuals participating in a research study or clinical trial that requires additional information or consent beyond the standard informed consent form.
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What is supplemental informed consent form?
A supplemental informed consent form is a document that provides additional information to participants in a research study, beyond what is included in the initial informed consent form. It helps ensure that participants are fully informed about changes or new risks associated with the study.
Who is required to file supplemental informed consent form?
Researchers or sponsors of a study that undergoes significant amendments or changes, which impact participant consent, are required to file a supplemental informed consent form.
How to fill out supplemental informed consent form?
To fill out a supplemental informed consent form, you should detail the new information that needs to be communicated, ensure clarity and comprehension, and provide all relevant details regarding the changes, including risks and benefits. It usually requires signatures from participants to acknowledge understanding.
What is the purpose of supplemental informed consent form?
The purpose of the supplemental informed consent form is to ensure that participants remain informed about their involvement in the study, particularly when there are substantial changes that could affect their willingness to participate.
What information must be reported on supplemental informed consent form?
The supplemental informed consent form must report any new risks, benefits, changes in procedures, and any other relevant information that could influence a participant's decision to continue in the study.
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