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INFORMED CONSENT FORM (ICF) Before agreeing to participate in this research study, it is important that you read the following explanation of this study. This statement describes the purpose, procedures,
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How to fill out an informed consent form (ICF):

01
Begin by reading the entire form carefully, ensuring that you understand all the information provided.
02
Fill in your personal details accurately, including your name, date of birth, and contact information.
03
Review the purpose of the study or procedure mentioned in the form and make sure you comprehend the risks and benefits involved.
04
If you have any concerns or questions about the study or procedure, reach out to the appropriate person or contact listed on the form for clarification.
05
Sign and date the form in the designated section to indicate your voluntary consent to participate in the study or procedure.
06
If needed, provide additional information or obtain signatures from witnesses as specified on the form.
07
Keep a copy of the signed consent form for your records.

Who needs an informed consent form (ICF)?

01
Any individual who is considering participating in a research study that requires informed consent will need to fill out an ICF.
02
Patients or participants involved in medical treatments or procedures, regardless of whether they are part of a clinical trial or not, generally need to provide informed consent by filling out an ICF.
03
Informed consent forms are also commonly required before participating in certain activities or services where potential risks or information are involved, such as sports, therapies, or legal agreements.
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Informed Consent Form (ICF) is a document used to provide potential participants with comprehensive information about a research study so they can make an informed decision about whether or not to participate.
Researchers and study sponsors are required to file Informed Consent Form (ICF) for participants in research studies.
Informed Consent Form (ICF) should be filled out by providing clear and detailed information about the study, risks and benefits, participant rights, and obtaining the participant's signature to indicate their informed consent.
The purpose of Informed Consent Form (ICF) is to ensure that participants are well-informed about the research study, its risks and benefits, and to obtain their voluntary consent to participate.
Informed Consent Form (ICF) should include information about the study objectives, procedures, risks, benefits, confidentiality, participant rights, contact information, and signature lines for the participant and researcher.
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