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Este documento permite a los padres/guardianes dar su consentimiento para que sus hijos participen en programas de Y, reconociendo los riesgos involucrados, y proporcionando la información necesaria
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How to fill out permission and informed consent

01
Start with a clear title identifying the purpose of the permission and informed consent form.
02
Provide a brief introduction explaining the study or procedure, its purpose, and the importance of consent.
03
Outline the procedure in detail, specifying what participants will be asked to do.
04
Include a section on potential risks and benefits of participating.
05
Describe how confidentiality will be maintained and how data will be used.
06
Clearly state that participation is voluntary and participants can withdraw at any time without penalty.
07
Provide space for participants to sign and date the form, indicating their consent.
08
Ensure participants receive a copy of the signed consent form for their records.

Who needs permission and informed consent?

01
Research participants involved in studies, surveys, or clinical trials.
02
Patients undergoing medical procedures or treatments.
03
Minors, which require parental or guardian consent.
04
Individuals providing personal data for research or other purposes.
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Permission and informed consent refer to the process of obtaining voluntary agreement from individuals to participate in a specific activity or research after providing them with all relevant information about the purpose, benefits, risks, and their rights.
Researchers, healthcare professionals, and any individuals or organizations conducting studies or procedures that involve human participants are required to file permission and obtain informed consent.
To fill out permission and informed consent, start by clearly stating the purpose and nature of the study or procedure, risks and benefits involved, confidentiality assurances, and the right to withdraw at any time. Then, provide space for signatures from the participant and, if necessary, a witness.
The purpose of permission and informed consent is to ensure that participants are fully informed about what they are agreeing to, protect their autonomy, and promote ethical standards in research and clinical practices.
The information that must be reported includes the study's purpose, procedures, potential risks and benefits, alternative options, confidentiality measures, and contact information for questions or concerns.
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