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Informed consent form:
Evaluation of Novartis Access in Kenya
Background
You are being asked to take part in this research study because you work at a health
facility that dispenses medications for
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How to fill out informed consent form
How to fill out informed consent form
01
Step 1: Read the entire informed consent form carefully to understand the purpose, risks, benefits, and procedures involved in the study or procedure.
02
Step 2: Provide your personal information accurately, including your name, address, contact details, and any relevant medical history.
03
Step 3: Ask any questions or seek clarification from the researcher or healthcare professional if you have any doubts or concerns about the study or procedure.
04
Step 4: Sign and date the informed consent form to indicate your voluntary agreement to participate or undergo the specific study or procedure.
05
Step 5: Keep a copy of the signed informed consent form for your records.
06
Step 6: If you change your mind at any point, inform the researcher or healthcare professional immediately and withdraw your consent.
Who needs informed consent form?
01
Informed consent forms are typically needed by individuals who are participating in research studies, clinical trials, medical procedures, or any situation where their voluntary agreement and understanding of the risks and benefits are required. This can include patients, research participants, and volunteers who are involved in various healthcare and scientific activities.
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What is informed consent form?
An informed consent form is a document that provides individuals with information about a study or procedure, allowing them to make an informed decision about participation.
Who is required to file informed consent form?
Researchers or institutions conducting studies involving human subjects are required to file informed consent forms.
How to fill out informed consent form?
To fill out an informed consent form, ensure all relevant information about the study is included, such as risks, benefits, procedures, and the participant's rights, and then have the participant sign it.
What is the purpose of informed consent form?
The purpose of the informed consent form is to ensure that participants understand the nature of the study, the risks involved, and their rights, thus protecting their autonomy.
What information must be reported on informed consent form?
The informed consent form must report information such as study purpose, procedures, risks, benefits, confidentiality, and the right to withdraw.
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