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I consent to participate in the research project and the following has been explained to me: the research may not be of direct benefit to me. my participation is completely voluntary. my right to withdraw from the study at any time without any implications to me.
Considerations in preparing the informed consent document: Elements of consent present. Complete explanations. Lay language. Protection of confidentiality. No unproven claims of effectiveness. Device studies include a statement that the study includes an evaluation of the safety of the test article.
Customize the downloaded template or new letter with your child's information, including their full name, date of birth, or any relevant identification details. Provide specific details about the consent, such as the event or activity your child is participating in and any related dates or duration.
I, ____________________________, confirm that I am the parent/guardian of _______________________. This is my written consent for _____________________________ to be employed by _________________. I certify that the herein stated is true and correct to the best of my knowledge and belief.
For an ethically valid consent, information provided to a research subject should include, but not be limited to: information about the health condition for which the research is proposed; details of the nature and purpose of the research; the expected duration of the subject's participation; a detailed description of ...