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INFORMED CONSENT FOR UNPERSON SERVICES DURING COVID-19 PUBLIC HEALTH CRISIS This document contains important information about our decision (yours and mine) to resume unperson services in light of
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Who needs research ethics and informed?

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Research ethics and informed consent are necessary for anyone participating in a research study, including:
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- Human subjects or participants involved in medical, psychological, sociological, or scientific research.
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- Individuals involved in clinical trials or experimental treatments.
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- Patients receiving medical treatments or procedures that involve research.
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Research ethics and informed consent are guidelines and procedures designed to ensure that research participants are treated ethically and informed about the research project they are participating in.
Researchers and institutions conducting research involving human subjects are required to file research ethics and informed consent forms.
Research ethics and informed consent forms can be filled out by providing detailed information about the research project, risks and benefits, confidentiality measures, and obtaining the participant's signature.
The purpose of research ethics and informed consent is to protect the rights and welfare of research participants and ensure that they are fully informed about the research project they are participating in.
Research ethics and informed consent forms must include information about the research project, potential risks and benefits, confidentiality measures, and the participant's rights.
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