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APPENDIX C1 SAMPLE CONSENT TO MEDICAL CARE & TREATMENT OF MINOR CHILD and EMERGENCY MEDICAL INFORMATION I hereby give permission that my child, may be given emergency treatment by a qualified staff
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How to fill out appendix c1 sample consent

How to Fill out Appendix C1 Sample Consent:
01
Read through the entire sample consent form carefully to understand the purpose and requirements.
02
Fill in the necessary personal information such as name, address, contact details, and date of birth in the designated fields.
03
Provide a brief explanation of the project or research study for which the consent form is required. Include details about the purpose, objectives, and any potential risks or benefits associated with participation.
04
Clearly state the voluntary nature of participation, ensuring that it is emphasized that individuals have the right to withdraw their consent at any time without consequences.
05
Specify the procedures involved, including any involvement of data collection, interviews, surveys, observations, or other activities. Ensure that the participants have a thorough understanding of what will be required from them.
06
Describe any confidentiality or privacy measures that will be implemented to protect the participants' information.
07
Include a section on risks and benefits, outlining any potential risks or discomfort that participants may experience during the study. Be transparent about any anticipated benefits or potential contributions to scientific knowledge.
08
Clearly explain the duration of participation and any anticipated follow-up or future contact.
09
If relevant to the study, provide information about compensation or incentives, if any, that participants may receive.
10
Include a section for participants to provide their signature, indicating their informed consent to participate in the study.
Who Needs Appendix C1 Sample Consent:
01
Individuals participating in research studies or projects that require their voluntary consent.
02
Researchers or institutions conducting studies or projects that involve human subjects and require documented consent.
03
Organizations or entities that need to obtain informed consent from individuals before collecting data, conducting interviews, surveys, or observations for their research or project.
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