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Ann Solid, Ph.D. 5970 Fairview Road Suite 412 Charlotte, NC 28210 Informed Consent Please read the following information carefully. Feel free to discuss any questions or concerns that may arise. Fees
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Who needs informed consent changes-1:

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Researchers or healthcare professionals who need to update or modify certain aspects of the informed consent previously obtained from study participants or patients.
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Ethical review boards or committees responsible for ensuring the ongoing compliance of research studies with ethical standards, who may request informed consent changes to be made based on their review and recommendations.
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Informed consent changes-1 refer to any modifications or updates made to the original informed consent form.
The principal investigator or researcher conducting the study is required to file informed consent changes-1.
To fill out informed consent changes-1, the researcher must clearly explain the changes made to the original informed consent form and provide a rationale for those changes.
The purpose of informed consent changes-1 is to ensure that participants are fully informed about any modifications or updates to the study protocol and to obtain their continued consent.
The information that must be reported on informed consent changes-1 includes details of the changes made, the reasons for those changes, and any potential impacts on the participants.
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