Get the free Informed Consent Form - Parkinson's Family Projects
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UNAFFECTED RELATIVESInformed Consent Form
Version 1.7
22/05/2018
Study: Parkinson's Families Project (PFP)
Chief Investigator: Professor How Morris. Principal Investigator: Professor How Morris
Name:
Address:DOB:Hospital:Hospital
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How to fill out informed consent form
How to fill out informed consent form
01
Read the informed consent form carefully and understand its contents.
02
Provide all necessary personal information such as name, age, address, and contact details.
03
Understand the purpose and nature of the study or medical procedure.
04
Ask any questions or seek clarifications from the authorized person if something is unclear.
05
Sign and date the form to indicate your consent to participate or undergo the procedure.
06
Keep a copy of the informed consent form for your reference.
Who needs informed consent form?
01
Informed consent forms are needed by anyone who is participating in a research study, clinical trial, medical procedure, or any activity that involves potential risks or benefits.
02
This includes patients, volunteers, research subjects, or anyone who is going to provide their consent for their personal data to be used for research purposes.
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What is informed consent form?
An informed consent form is a document that outlines the details of a study or treatment, ensuring that participants understand what is involved and agree to participate voluntarily.
Who is required to file informed consent form?
Researchers, healthcare providers, and organizations conducting studies or clinical trials involving human participants are required to file informed consent forms.
How to fill out informed consent form?
To fill out an informed consent form, provide clear information about the study or treatment, including its purpose, procedures, risks, benefits, and confidentiality issues, and then ensure the participant reviews and signs the form.
What is the purpose of informed consent form?
The purpose of an informed consent form is to ensure that participants are adequately informed about the study or treatment, allowing them to make a knowledgeable decision about their participation.
What information must be reported on informed consent form?
The informed consent form must report information such as the study's purpose, procedures, potential risks and benefits, confidentiality assurances, and participant rights.
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