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SAMPLE INFORMED CONSENT WANT 2008-02: Phase I study of in combination with 13-cis-retinoic acid in patients with refractory/recurrent neuroblastomas A New approach to Neuroblastomas Therapy (WANT)
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How to fill out a sample informed consent form:

01
Begin by carefully reading through the entire consent form to ensure you understand its contents.
02
Provide your personal information, such as your name, contact details, and any other required identification details.
03
Clearly state the purpose of the research or study for which you are being asked to provide consent.
04
Familiarize yourself with any potential risks or benefits associated with participating in the research.
05
Make sure to understand the confidentiality policies regarding your personal information and how it will be used.
06
If there are any potential conflicts of interest or financial disclosures, ensure they are accurately stated.
07
Carefully review any required procedures or tasks you may be required to perform during the course of the research.
08
If you have any questions or concerns, it is crucial to address them with the responsible party or the research team.
09
Once you have a clear understanding of the consent form and are comfortable proceeding, sign and date the document.
10
Keep a copy of the consent form for your records.

Who needs a sample informed consent form?

01
Researchers or organizations conducting studies or research involving human participants.
02
Medical professionals who require patient consent for specific procedures, treatments, or participation in clinical trials.
03
Educational institutions conducting research involving their students or staff members.
04
Non-profit organizations conducting surveys, interviews, or data collection involving individuals.
05
Any person or entity involved in research, studies, or activities that require ethical approval and participant consent.
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Sample informed consent nant is a document provided to participants outlining the purpose, risks, benefits, and procedures of a study or research project, and obtaining their voluntary agreement to participate.
Researchers conducting studies or research projects involving human participants are required to file sample informed consent nant.
Sample informed consent nant is typically filled out by providing detailed information about the study, risks, benefits, procedures, confidentiality measures, and obtaining signatures from the participants and researchers.
The purpose of sample informed consent nant is to ensure that participants are fully informed about the study they are participating in, their rights are protected, and their voluntary agreement is obtained.
Sample informed consent nant must include information about the study purpose, procedures, risks, benefits, confidentiality measures, contact information of the researchers, and participant rights.
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