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Apart A: Informed Consent, Release Agreement, and Authorization High adventure base participants:Full name: Date of birth: Expedition/crew No.: or staff position: Informed Consent, Release Agreement,
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How to fill out part a informed consent

01
Begin by stating the name of the study or project for which informed consent is being requested.
02
Provide a brief description of the purpose and nature of the study or project.
03
Clearly explain the procedures involved in the study or project, including any risks or benefits.
04
Describe any alternatives to participating in the study or project.
05
Ensure that the participant understands that their participation is voluntary and that they have the right to refuse or withdraw at any time.
06
Provide contact information for the researcher or organization conducting the study or project, in case the participant has any questions or concerns.
07
Include a statement about the confidentiality of the participant's information and how it will be used.
08
Leave space for the participant to sign and date the informed consent form.
09
Provide a copy of the informed consent form to the participant for their records.
10
Keep a record of all informed consent forms signed by participants.

Who needs part a informed consent?

01
Part A informed consent is needed for any individuals who are being asked to participate in a study or project that involves gathering data or conducting research. This includes both human subjects and potential participants who may be affected by the study or project in some way.
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Part A informed consent is a process in which a participant is given all the necessary information about a research study before deciding to participate.
Researchers conducting a study requiring informed consent are required to file Part A informed consent.
Part A informed consent is filled out by providing detailed information about the research study, risks and benefits of participation, and ensuring the participant understands and agrees to participate.
The purpose of Part A informed consent is to ensure that participants have all the information necessary to make an informed decision about participating in a research study.
Part A informed consent must include details about the research study, risks and benefits, confidentiality, voluntary participation, and contact information for questions.
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