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INFORMED CONSENT FORMS FOR KIT AND FED SESSIONS PANDORA GROUP 11th Floor Ramon Magsaysay Center Rojas Boulevard, Manila RESEARCH PROJECT: SURGE Evaluation in support of the USAID Claimed project in
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01
Read the entire informed consent form thoroughly before filling it out.
02
Make sure you understand the purpose, procedures, risks, and benefits of the study or treatment.
03
Provide accurate personal information such as your name, age, and contact details.
04
If you have any questions or concerns, talk to the research team or healthcare provider before signing the form.
05
If you agree to participate, sign and date the form.
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Keep a copy of the informed consent form for your records.
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Ask for a copy of any other documents you need to review or sign.
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Remember that giving informed consent is voluntary, and you have the right to withdraw your consent at any time.

Who needs informed consent forms for?

01
Informed consent forms are required for individuals who are participating in research studies, clinical trials, medical procedures, or any form of treatment that involves potential risks or uncertainties.
02
These forms ensure that individuals have been provided with all the necessary information to make an informed decision about their participation or treatment.
03
In some cases, informed consent forms may also be needed for minors, individuals with limited decision-making capacity, or individuals who are unable to provide consent due to health conditions.
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Informed consent forms are used to ensure that participants in research studies understand the nature of the study, their role in it, and any potential risks, benefits, and alternatives before agreeing to participate.
Researchers and institutions conducting studies involving human participants are required to file informed consent forms as part of the ethics review process.
To fill out informed consent forms, provide clear and concise information about the study, including its purpose, procedures, risks, benefits, confidentiality, and obtaining a signature from the participant or their legal guardian.
The purpose of informed consent forms is to protect the rights and welfare of research participants by ensuring they have all necessary information to make an informed decision about their participation.
Informed consent forms must report information such as study purpose, procedures, duration, risks and benefits, confidentiality measures, and the right to withdraw at any time without penalty.
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