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INFORMED CONSENT FORM FOR STORAGE OF HUMAN BIOLOGICAL MATERIAL FOR RESEARCH PURPOSES1 BIOMEDICAL RESEARCH ETHICS COMMITTEE, UNIVERSITY OF ZULU NATAL×Name of Project×The Document consists of two
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How to fill out informed consent form for

01
Read the informed consent form carefully and understand its contents.
02
Provide all necessary personal information, such as name, address, and contact details.
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Clearly indicate your consent to participate in the specific activity or study.
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Ensure that you sign and date the form to acknowledge your understanding and agreement.
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Retain a copy of the completed and signed informed consent form for your records.

Who needs informed consent form for?

01
Informed consent forms are typically required for individuals participating in research studies or clinical trials.
02
Medical procedures that carry potential risks or require patient agreement often require an informed consent form.
03
Participants in educational activities, such as workshops or training programs, may need to complete an informed consent form.
04
Certain professional services, such as counseling or therapy sessions, may also involve the use of an informed consent form.
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Other situations where informed consent forms may be necessary include participating in legal agreements, signing contracts, or undergoing invasive or experimental treatments.

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Informed consent form is used to ensure that patients or participants have all the necessary information needed to make an informed decision regarding their participation in a study or procedure.
Researchers, healthcare professionals, or individuals conducting a study or procedure are required to file informed consent form for.
To fill out an informed consent form, one must include all the necessary information about the study or procedure, risks and benefits, alternatives, and allow individuals to ask questions before signing.
The purpose of informed consent form is to protect the rights and well-being of patients or participants by ensuring they have all the necessary information to make an informed decision.
Information such as study or procedure details, risks and benefits, alternatives, confidentiality, contact information, and ability to withdraw from the study must be reported on an informed consent form.
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