Disclaimer: This consent form was not used in these experiments 2026

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  1. Click ‘Get Form’ to open it in the editor.
  2. Begin by reviewing the introductory section, which outlines the purpose of the consent form. Ensure you understand that this form is not associated with the experiments mentioned.
  3. Fill in your name as the Parent or Guardian in the designated field. This identifies you as the individual providing consent for your child's participation.
  4. Carefully read through each paragraph detailing the risks and benefits associated with mercury/silver fillings. Make notes if necessary for any questions you may have.
  5. Sign and date the form at the bottom to indicate your agreement and understanding of what participation entails.
  6. Submit the completed form by following any provided instructions for return, ensuring it reaches the appropriate party for processing.

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The only exceptions are: in an emergency when the patient lacks capacity and the patients express wishes are unknown; or where the law otherwise allows or requires treatment to be given without consent.
Informed consent is more than merely a signature on a document; it is a communication process between the clinician and the patient. This process ensures that the patient is fully informed about the nature of the procedure or intervention, the potential risks and benefits, and the alternative treatments available.
In certain cases, federal regulations allow the IRB to waive the requirement to obtain any informed consent. Most complete waivers of consent involve studies in which there are minimal risks to subjects, but complete waivers are also possible in emergency care and other limited circumstances.
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