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IRB Approved Consent Release Date: 05/23/2012 Consent Expiration Date: 05/22/2013 6585a Informed Consent Protocol Title: REPOSITORY OF DATA AND SPECIMENS FOR MERKEL CELL CARCINOMA RESEARCH (IRB #6585)
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How to fill out 6585a informed consent:

01
Start by carefully reading the entire document to understand the purpose and requirements of the informed consent form.
02
Provide accurate and complete personal information, such as your name, date of birth, and contact details.
03
Clearly state the purpose of the study or procedure for which the informed consent is being obtained.
04
Understand and acknowledge the potential risks and benefits associated with participating or undergoing the study or procedure.
05
Sign and date the form to indicate that you fully understand and voluntarily consent to participate or undergo the study or procedure.
06
Ensure that any questions or concerns you may have are addressed by the responsible party, such as the researcher, doctor, or study coordinator.

Who needs 6585a informed consent:

01
Individuals who are participating in a research study that requires informed consent.
02
Patients who are undergoing a medical procedure that necessitates informed consent.
03
Individuals who are involved in any activity that may carry potential risks and requires informed consent as a legal and ethical requirement.
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6585a informed consent refers to the process where individuals are provided with all relevant information regarding a medical procedure, treatment, or research study, and are given the opportunity to agree or refuse to participate.
Healthcare providers, researchers, or institutions conducting medical procedures, treatments, or research studies are required to obtain and file 6585a informed consent from individuals participating in these activities.
To fill out 6585a informed consent, individuals must be presented with all necessary information about the procedure, treatment, or study in a clear and understandable manner. Individuals must then sign the consent form indicating their agreement.
The purpose of 6585a informed consent is to ensure that individuals are fully informed about the risks, benefits, and alternatives of a medical procedure, treatment, or research study before making a decision to participate.
6585a informed consent must include details on the procedure, treatment, or study being conducted, potential risks and benefits, alternative options, confidentiality measures, and the right to withdraw consent at any time.
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Relevant keywords

2012 2013 WASHINGTON MCC NGHIEM IRB 6585a PHD MERKEL HUTCHINSON FHCRC Hansen Institutes Archival contraindications generalized milliliters Collaborative CARCINOMA Protections REPOSITORY collaborators Additionally institutional collaborating participant No

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