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SAMPLE INFORMED CONSENT A Phase I Study of Intravenous (Emulsion) Fenretinide (4HPR, NSC 374551) in Children with Recurrent or Resistant Neuroblastomas (IND #70,058) A New Approaches to Neuroblastomas
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To fill out a sample informed consent form, you can follow these steps:

01
Begin by carefully reading the entire consent form to understand its purpose and the information it requires.
02
Fill in your name and contact information in the designated fields. This ensures that you can be identified as the participant or the legal authority responsible for the individual.
03
Provide any demographic information that is requested, such as age, gender, and ethnicity. This helps researchers analyze data based on different characteristics.
04
Review the study or procedure description thoroughly, ensuring that you understand the purpose, risks, benefits, and any alternatives involved.
05
If there are any specifics regarding participation expectations, obligations, or requirements, make sure to fill them out accordingly.
06
If there are any sections that require signatures, read them carefully and sign as necessary. This indicates your voluntary participation in the study or procedure.
07
If there is a section for witness signatures, ensure that it is completed by an objective individual who has observed your signing process.
08
Finally, retain a copy of the fully completed informed consent form for your records.
As for who needs a sample informed consent form, it typically applies to individuals who participate in research studies, medical procedures, clinical trials, or similar activities where informed consent is necessary. This can include patients, volunteers, or participants of various demographics. The purpose is to ensure that individuals have a clear understanding of the study or procedure and can make an informed decision about their participation.
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Sample informed consent is a document that outlines the risks and benefits of participating in a research study.
Researchers or institutions conducting the research study are required to file sample informed consent with the appropriate ethics committee or regulatory body.
Sample informed consent should be filled out by providing all necessary information about the study, including the purpose, procedures, risks, benefits, and participant rights.
The purpose of sample informed consent is to ensure that participants understand and voluntarily agree to participate in a research study.
Sample informed consent must include information about the study objectives, procedures, risks, benefits, confidentiality, and participant rights.
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