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NCI CIRB Protocol: NRG GY012 Consent Version Number: Amendment 1 Consent Version Date: 011519 Consent Implementation Date: 021519-Page 1 of 18NRG Oncology GUN Informed Consent Template Research Study
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Obtain the NRG Oncology GYN informed consent form.
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Read the form thoroughly to understand the risks, benefits, and procedures involved.
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Fill out all the required personal information accurately.
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Initial and sign the form indicating your consent to the GYN oncology treatment.

Who needs nrg oncology gyn informed?

01
Patients who are undergoing GYN oncology treatment
02
Patients who have been diagnosed with gynecological cancer
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NRG Oncology GYN Informed is a form designed to collect specific information regarding gynecologic oncology cases.
Medical professionals involved in the treatment of gynecologic oncology cases are required to fill out the NRG Oncology GYN Informed form.
The NRG Oncology GYN Informed form can be filled out electronically or manually by providing detailed information about the gynecologic oncology case.
The purpose of the NRG Oncology GYN Informed form is to collect essential data on gynecologic oncology cases for research and quality improvement purposes.
Information such as patient demographics, diagnosis details, treatment received, and outcomes of the gynecologic oncology case must be reported on the NRG Oncology GYN Informed form.
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