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6.1. Informed Consent Form
6.1.1. English Version
NORWEGIAN UNIVERSITY OF LIFE SCIENCES, DEPARTMENT OF FOOD
SAFETY AND INFECTION BIOLOGY
IDNOConsent to participate in a study
Greetings! My name is
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Read through the form carefully to understand the information and requirements.
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Fill out all the necessary fields accurately and truthfully.
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Sign and date the form to indicate your acknowledgment and consent.
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If there are any sections you do not understand, seek clarification from a healthcare provider or research staff before signing.
Who needs 61 informed consent form?
01
Researchers conducting medical or scientific studies that involve human subjects.
02
Patients or participants who are considering participating in a research study or clinical trial.
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What is 61 informed consent form?
The 61 informed consent form is a document that ensures individuals are fully informed about a study or procedure and consent to participate voluntarily.
Who is required to file 61 informed consent form?
Researchers and institutions conducting studies that require informed consent from participants are required to file the 61 informed consent form.
How to fill out 61 informed consent form?
To fill out the 61 informed consent form, one must provide detailed information about the study, including its purpose, procedures, risks, benefits, and assurances of confidentiality, as well as obtaining participant signatures.
What is the purpose of 61 informed consent form?
The purpose of the 61 informed consent form is to ensure that participants understand what they are agreeing to, protecting their autonomy and rights.
What information must be reported on 61 informed consent form?
The information that must be reported includes the study's purpose, potential risks and benefits, procedures involved, duration, and contact information for questions or concerns.
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