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DPHHSMA38 (Rev. 11/2016) STATE OF MONTANA DEPARTMENT OF PUBLIC HEALTH AND HUMAN SERVICES INFORMED CONSENT TO STERILIZATION NOTICE: YOUR DECISION AT ANY TIME NOT TO BE STERILIZED WILL NOT RESULT IN
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Who needs attachment d informed consent?
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Anyone who is participating in a research study or clinical trial that requires informed consent.
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What is attachment d informed consent?
Attachment D informed consent is a document that outlines the risks, benefits, and procedures involved in participating in a research study or medical treatment.
Who is required to file attachment d informed consent?
Researchers, healthcare providers, or individuals conducting a study or treatment that involves human subjects are required to file attachment D informed consent.
How to fill out attachment d informed consent?
Attachment D informed consent should be filled out by providing clear and detailed information about the study or treatment, including risks, benefits, and procedures, and obtaining the signature of the participant or their legal representative.
What is the purpose of attachment d informed consent?
The purpose of attachment D informed consent is to ensure that participants are fully informed about the study or treatment they are involved in, and to obtain their voluntary agreement to participate.
What information must be reported on attachment d informed consent?
Attachment D informed consent should include information about the study or treatment, risks, benefits, procedures, confidentiality, contact information, and any compensation provided to participants.
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