NCI BOLD Task Force IMAGING Common Data Elements (CDE) – MODULE 1 1. Date of Imaging: (mm-dd-yyyy) 2. Date of Interpretation:

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• Pathology
• Ribbon symbolism
• Mammography
• Projectional radiography
• Magnetic resonance imaging
• Breast cancer
• Carcinoma
• Medical ultrasonography
• Medicine
• Cancer screening
• Biopsy

Working Group Rosters: NCI Concise Informed Consent Template Project Role Working Group 1 (Beginning of template – background, required tests, intervention sections) Working Group 2 (Risks and benefits sections) Workin

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• Biology
• SWOG
• Cancer and Leukemia Group B
• American College of Surgeons Oncology Group
• Eastern Cooperative Oncology Group
• Cancer Trials Support Unit
• Cancer organizations
• Health
• Research

NCI BOLD Task Force Common Data Elements (CDE) – Surgical Patient ID#:___________________________ Tumor Assessment Tumor Singularity (check one)  Solitary # of Ipsilateral tumors______  >1 Quadrant

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• Surgical oncology
• Breast cancer
• Ribbon symbolism
• Mastectomy
• Lumpectomy
• Radical mastectomy
• Breast implant
• Breast reconstruction
• Quadrantectomy
• Medicine
• Surgery
• Breast surgery

February 15, 2013 Dear IRB Chairs and Members, The National Cancer Institute (NCI) has completed an initiative to revamp its Consent Form Template. The NCI has revisited the content of consent forms to address concerns o

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• Autonomy
• Research ethics
• Informed consent
• Belmont Report
• Consent
• Human subject research
• Institutional review board
• Cancer and Leukemia Group B
• Ethics
• Medical ethics
• Clinical research

CONFIDENTIAL DISCLOSURE AGREEMENT This Agreement is made by and between the Institution Name, having a place of business at address, (“Institution”) with Dr. PI name as employee of Institution, and Patient/family me

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• Research
• Data
• Clinical trial
• Design of experiments
• Drug discovery
• Pharmacology
• Protocol
• Communications protocol
• Pharmaceutical industry
• Clinical research
• Science

February 15, 2013 Dear Investigator: The NCI’s Consent Form Template has been revised to result in shorter, more concise consent forms for NCI-sponsored trials. Studies have shown that longer consent forms are more int

Source URL: ctep.cancer.gov

• Cancer organizations
• Clinical research
• Research
• Research ethics
• Belmont Report
• Human subject research in the United States
• Informed consent
• Consent
• National Cancer Institute
• Medicine
• Medical ethics
• Ethics

Instructions for Building “Possible Side Effects” Tables for Informed Consent Forms Commercially Available Agents (Single Agents) Instructions Version Date: January 2012, v1 Note to informed consent form authors: MIC

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• Injuries
• Ethics
• Informed consent
• Sexual intercourse
• Vaginal bleeding
• Internal bleeding
• Consent
• Behavior
• Human behavior
• Medicine

Pharmaceutical Management Branch Cancer Therapy Evaluation Program, DCTD, NCI Policy and Guidelines for INVESTIGATIONAL AGENT ORDERING Policy: Active CTEP registered investigators or their authorized shipping designees a

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• Food and Drug Administration
• Design of experiments
• Pharmacology
• Business
• Email
• Clinical trial
• Order processing
• Online shopping
• Clinical research
• Science
• Research

PDF Document

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Pregnancy Information Form-GNE-edit-jhm-2.pdf

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