| Acronyms |
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| ACR American College of Radiology, http://www.acr.org/ |
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| ADR Adverse Drug Reaction |
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| B |
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| BCOP Board Certified Oncology Pharmacist |
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| C |
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| CABG Cardiac/Coronary Artery Bypass Graft |
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| CALGB Cancer and Leukemia Group B, http://www.calgb.org/ |
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| CCOP Childhood Cancer Ombudsman Program or Community Clinical
Oncology Program, |
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| http://www.childhoodbraintumor.org/ombuds.html |
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| CCSG Children's Cancer Study Group (now known as CCG) |
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| CFR Code of Federal Regulations |
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| CIM Certified IRB Manager |
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| CIP Certified IRB Professional |
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| CIRB Central Institutional Review Board of the NCI,
http://www.ncicirb.org |
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| CLIA Clinical Laboratory Improvement Act/Amendment |
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| CME Continuing Medical Education |
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| COC Certificate of Confidentiality |
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| COG Cooperative Oncology Groups funded by NCI: See also CCG,
COG, ECOG, GOG, RTOG, POG, CALGP, |
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| and NABTC |
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| CPA Cooperative Project Assurance |
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| CRA Clinical Research Associate |
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| CRC Clinical Research Coordinator |
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| CRO Clinical Research Organization/Contract Research
Organization |
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| D |
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| DHEW Department of Health, Education and Welfare (no longer
exists) |
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| DIA Drug Information Association |
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| DMC Data Monitoring Committee |
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| DOE (US) Department of Education, http://www.ed.gov/ |
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| DSMB Data Safety Monitoring Board |
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| E |
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| EBM Evidence-based medicine |
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| EQUIC Enhancing Quality of Informed Consent |
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| F |
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| FERPA Family Educational Rights and Privacy Act (aka the Buckley
Amendment), |
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| http://www.ed.gov/legislation/FedRegister/proprule/1999-2/060199e.html |
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| FWA Federal Wide Assurance |
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| G |
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| GCP Good Clinical Practice |
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| GeMCRIS Genetic Modification Clinical Research Information System |
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| GMP Good Manufacturing Practice |
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| GTSAB Gene Transfer Safety Assessment Board |
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| H |
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| HCFA Health Care Financing
Administration (now known as CMS; Centers for Medicare and Medicaid
Services) |
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| http://cms.hhs.gov/medicaid/default.asp |
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| HDE Humanitarian Device Exemption (what a HUD is classified as) |
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| HIPAA Health Insurance Portability and Accountability Act |
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| HMO Health Maintenance Organization |
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| HPA Human Protections Administrator |
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| HRP Human Research Protections |
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| HREC Human Research Ethics Committee |
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| HRT Hormone Replacement Therapy |
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| HSR Health Services Research |
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| HUD Humanitarian Use Device |
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| I |
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| IB Investigator's Brochure |
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| IBC Institutional Biohazard Committee (needed in gene transfer
research). Also Inflammatory Breast Cancer |
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| ICD Informed Consent Document |
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| ICF Individual Consent Form or Institutional Consent Form |
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| ICH International Conference on Harmonization of Technical
Requirements for Registration of Pharmaceuticals |
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| http://www.ich.org/ |
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| ICH-GCP International Conference on Harmonization Good Clinical
Practice, |
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| http://64.233.161.104/search?q=cache:dpsrSuzRy-QJ:www.fda.gov/cder/guidance/959fnl.pdf+ICH+GCP&hl=en |
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| ICS Informed Consent Statements |
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| IDB Investigator's Drug Brochure |
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| IDE Investigational Device Exemption |
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| IEC Institutional Ethics Committee/Independent Ethics Committee |
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| IND Investigational New Drug (application) |
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| IRB Institutional Review Board |
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| IRSG Intergroup Rhabdomyosarcoma Study Group |
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| J |
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| JIT Just in Time (procedure) |
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| L |
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| LAR Legally Authorized Representative |
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| LEP Limited English Prociency |
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| LTF Long-Term Facilitation/Long-Term Fellowship |
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| LTF Subjects Lost to Follow-up Subjects |
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| M |
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| MI Myocardial Infarction (heart attack) |
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| MPA Multiple Project Assurance |
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| MSM Men who have Sex with Men |
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| NABTC North American Brain Tumor Consortium,
http://www.nabtc.org/ |
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| NAIAD Nerve Agent Immobilized Enzyme Alarm & Detector |
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| NCPHSBBR National Commission for the Protection of Human Subjects of
Biomedical and Behavioral Research |
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| NCQA National Committee for
Quality Assurance (currently responsible for accreditation of VA research
programs) |
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| http://www.ncqa.org/ |
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| NICU Neonatal Intensive Care Unit |
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| NIA Nonaffiliated Investigator Agreement |
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| NSAID Non-Steroid Anti-Inflammatory Drug |
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| O |
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| OLES Open Label Extension Studies |
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| P |
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| PCP Primary Care Physician |
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| PCR Polymerase Chain Reaction (technique to replicate fragment
of DNA for genetic analysis) |
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| PDUFA Prescription Drug User Fee Act of 1992 |
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| PHI Private Healthcare Information/Public Health
Information/Protected Health Information |
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PHS Public Health Service
(see also USPHS United States Public Health Service), |
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| http://www.hhs.gov/pharmacy/pp/DHHSpresent/ |
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| PI Principal Investigator |
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| P&P Policies and Procedures |
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| Q |
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| QIC Quality Improvement Committee |
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| QIP Quality Improvement Program |
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| R |
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| RAC Recombinant-DNA Advisory Committee |
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| RCO Regulatory Compliance Officer |
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| RCR Responsible Conduct of Research |
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| RCT Randomized Control Trial |
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| REB Research Ethics Board |
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| S |
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| SAE Serious Adverse Events |
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| SAP Suspect Adverse Reaction |
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| SBIR Small Business Innovative Research |
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| SCID Severe Combined Immunodeficiency Disease |
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| SMO Site Management Organization |
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| SOP Standard Operating Procedure |
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| SPA Single Project Assurance |
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| SR Safety Report/Significant Risk |
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| SRO Sponsored Research Office |
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| T |
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| U |
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| URI Upper Respiratory Infection |
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| V |
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| VPR Vice President for Research |
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| W |
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| qq |
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qq |
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| Columbia University Medical Center |
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| (IRB) |
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