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Get the free INFORMED CONSENT STATEMENT AND OFFICE POLICY 112014.doc

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1DBTCenterofOrangeCounty 369SanMiguelDrive,Suite200 Newport Beach,CA92660 Phone9494807767:Fax94920919776200ECanyonRimRoad,Suite212 AnaheimHills,CA92807INFORMEDCONSENTSTATEMENTANDOFFICEPOLICY ThefollowingstatementanswerssomeimportantquestionsconcerningtheDBTCenterofOrangeCounty
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Who needs informed consent statement and?

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Anyone who is participating in a research study or clinical trial.
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Patients undergoing medical procedures where informed consent is required.
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Individuals involved in certain activities that may have associated risks and require acknowledgement of understanding and agreement.
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An informed consent statement is a document that outlines the necessary information provided to individuals about the risks, benefits, and purpose of a procedure or study, enabling them to make an educated decision about their participation.
Researchers or organizations conducting studies involving human participants are required to file an informed consent statement.
To fill out an informed consent statement, one should include details such as the purpose of the study, procedures involved, risks and benefits, confidentiality measures, and the participant's rights, along with a signature section for the participant.
The purpose of an informed consent statement is to ensure that participants are fully aware of what their participation involves and to safeguard their autonomy and rights in the research process.
The informed consent statement must report information including the study's purpose, procedures, possible risks and benefits, confidentiality assurances, and the participant's right to withdraw.
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