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Rockefeller University Institutional Review Board IRB NUMBER: JGN0853 IRB APPROVAL DATE: 06/05/2015 IRB EXPIRATION DATE: 06/04/2016 Clinical Investigation Consent Form The Rockefeller University Hospital
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How to fill out clinical investigation consent form
How to fill out a clinical investigation consent form:
01
Start by carefully reading and understanding the purpose and nature of the clinical investigation. This will help you make an informed decision about participating.
02
Provide your personal information accurately, including your full name, date of birth, address, and contact details. This information is essential for identification and communication purposes.
03
Review the objectives, procedures, and potential risks and benefits associated with the clinical investigation. It is important to have a clear understanding of what you are consenting to.
04
Carefully read through the informed consent document, paying close attention to each section. If you have any questions, don't hesitate to ask the investigator or study personnel for clarification.
05
Sign and date the consent form. This indicates your voluntary participation and agreement to the terms outlined in the document.
06
If applicable, provide information about your health history, medications you are currently taking, and any allergies or previous adverse reactions to medications or treatments. This information will help researchers determine your eligibility for the study.
07
Keep a copy of the signed consent form for your records. It is important to have a copy of the document in case you need to refer to it in the future.
Who needs a clinical investigation consent form?
01
Individuals who are considering participating in clinical investigations or research studies involving human subjects generally need to fill out a clinical investigation consent form.
02
Patients or volunteers who meet the eligibility criteria and agree to participate in a clinical investigation or research study will be required to provide informed consent by signing the consent form.
03
The purpose of the consent form is to ensure that participants have sufficient information about the study, its potential risks and benefits, and to enable them to make an informed decision about their participation. Therefore, anyone who meets the criteria and wishes to participate needs to fill out the consent form.
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What is clinical investigation consent form?
The clinical investigation consent form is a document that outlines the purpose, risks, and procedures of a clinical trial, and is used to obtain informed consent from participants.
Who is required to file clinical investigation consent form?
Principal Investigators and sponsors of clinical trials are required to file the clinical investigation consent form.
How to fill out clinical investigation consent form?
The clinical investigation consent form must be filled out by including all relevant information about the trial, risks, benefits, and participant rights.
What is the purpose of clinical investigation consent form?
The purpose of the clinical investigation consent form is to ensure that participants are fully informed about the trial before agreeing to participate.
What information must be reported on clinical investigation consent form?
The clinical investigation consent form must report information about the trial objectives, procedures, risks, benefits, and participant rights.
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