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{"id":"1d9fbe912b5b2f43f5c9bcd3dd016e23","key":"21 CFR Part 11","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd016e23","_rev":"1-b9c940c754980f35d7ba2c83e4a1f550","Acronym":"21 CFR Part 11","Name":"Electronic Records; Electronic Signatures","Description":"The regulations in this part set forth the criteria under which the agency considers electronic records, electronic signatures, and handwritten signatures executed to electronic records to be trustworthy, reliable, and generally equivalent to paper records and handwritten signatures executed on paper.","Link1":"21 CFR Part 11 Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?cfrpart=11","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Pharma/Medical Device","Regulator":"FDA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd013ede","key":"21 CFR Part 210","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd013ede","_rev":"1-6eff7ff0465e66063e3ea9864d776ff6","Acronym":"21 CFR Part 210","Name":"Current Good Manufacturing Practice In Manufacturing, Processing, Packing, Or Holding Of Drugs","Description":"The regulations in this part contain the minimum current good manufacturing practice for methods to be used in, and the facilities or controls to be used for, the manufacture, processing, packing, or holding of a drug to assure that such drug meets the requirements of the act as to safety, and has the identity and strength and meets the quality and purity characteristics that it purports or is represented to possess.","Link1":"21 CFR Part 210 Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?cfrpart=210","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Pharma","Regulator":"FDA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd014786","key":"21 CFR Part 211","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd014786","_rev":"1-b02ba2bf14e806057ee2973fa717cf4f","Acronym":"21 CFR Part 211","Name":"Current Good Manufacturing Practice For Finished Pharmaceuticals","Description":"The regulations in this part contain the minimum current good manufacturing practice for preparation of drug products for administration to humans or animals.","Link1":"21 CFR Part 211 Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?cfrpart=211","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Pharma","Regulator":"FDA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd015100","key":"21 CFR Part 820","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd015100","_rev":"1-a20cca01f983a0fd1e6dec798d8644b8","Acronym":"21 CFR Part 820","Name":"Quality System Regulation","Description":"Current good manufacturing practice (CGMP) requirements are set forth in this quality system regulation. The requirements in this part govern the methods used in, and the facilities and controls used for, the design, manufacture, packaging, labeling, storage, installation, and servicing of all finished devices intended for human use. The requirements in this part are intended to ensure that finished devices will be safe and effective and otherwise in compliance with the Federal Food, Drug, and Cosmetic Act (the act). ","Link1":"21 CFR Part 820 Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?cfrpart=820","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Pharma","Regulator":"FDA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd0007c9","key":"AICC","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd0007c9","_rev":"1-e24bdea0802765bdeef4f9029bd248f8","Acronym":"AICC","Name":"Aviation Industry CBT Committee","Description":"The Aviation Industry CBT Committee is a nonprofit, membership-driven consortium dedicated to helping the training community get the most out of training technology.  We do that by bringing together trainers, courseware developers, software vendors, simulator designers and airframe manufacturers to develop standards, technology recommendations and analysis of best practices.","Link1":"AICC Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://aicc.org/joomla/dev/","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Airline","Regulator":""}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd001629","key":"ATOS","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd001629","_rev":"1-121af8afe784dff422bc43f967559f20","Acronym":"ATOS","Name":"Air Transport Oversight System","Description":"The Air Transportation Oversight System (ATOS) implements FAA policy by providing safety controls (i.e., regulations and their application) of business organizations and individuals that fall under FAA regulations. Three major functions further define the oversight system: design assessment, performance assessment, and risk management.","Link1":"ATOS Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.faa.gov/about/initiatives/atos/","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Airline","Regulator":"FAA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00bcf4","key":"Basel II","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00bcf4","_rev":"1-0654a89828a9f86bdf2851551fac66c9","Acronym":"Basel II","Name":"International Convergence of Capital Measurement and Capital Standards: a Revised Framework","Description":"The International Convergence of Capital Measurement and Capital Standards: a Revised Framework, or the “Basel II Framework,” offers a new set of standards for establishing minimum capital requirements for banking organisations. It was prepared by the Basel Committee on Banking Supervision, a group of central banks and bank supervisory authorities in the G10 countries, which developed the first standard in 1988.","Link1":"Basel II Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.bis.org/publ/bcbs107.htm","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Financial","Regulator":"BIS"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00cb3d","key":"BSA","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00cb3d","_rev":"1-1219458029a5e8a687b4f24a097244f1","Acronym":"BSA","Name":"Bank Secrecy Act","Description":"The Bank Secrecy Act of 1970 (or BSA, or otherwise known as the Currency and Foreign Transactions Reporting Act) requires financial institutions in the United States to assist U.S. government agencies to detect and prevent money laundering. Specifically, the act requires financial institutions to keep records of cash purchases of negotiable instruments, and file reports of cash purchases of these negotiable instruments of more than $10,000 (daily aggregate amount), and to report suspicious activity that might signify money laundering, tax evasion, or other criminal activities. Many banks will no longer sell negotiable instruments when they are purchased with cash, requiring the purchase to be withdrawn from an account at that institution.","Link1":"Wikipedia","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://en.wikipedia.org/wiki/Bank_Secrecy_Act","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Financial","Regulator":"US Congress"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd001a50","key":"CAS/CASS","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd001a50","_rev":"1-d90b8df74fa8ac727be7b76a0c8bf321","Acronym":"CAS/CASS","Name":"Continuing Analysis & Surveillance System","Description":"Since 1964, all air carriers have been required by regulation to conduct continuous evaluations of their maintenance programs. Specifically, Title 14 Code of Federal Regulations (CFR) Parts 121.373 and 135.431 require air carriers to establish a Continuing Analysis and Surveillance System (CASS) to evaluate, analyze, and correct deficiencies in the performance and effectiveness of their inspection and maintenance programs.   While the regulation governing CASS is short, its sparse language nonetheless requires a complex system.  Each CASS must set high goals, and the Federal Aviation Administration (FAA) is empowered by the regulations to require changes to an air carrier’s maintenance program if it shows signs of weakness.","Link1":"CAS/CASS Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"https://hfskyway.faa.gov/(A(4vy9onHDygEkAAAAMjNiMWJmMzktODkyZi00YTExLWIyM2MtMTE4MTY3NmYzY2E3ePZ2EDFXCWbSRl3xlJVF1bY24D81))/HFTest/Bibliography%20of%20Publications%5CHuman%20Factor%20Maintenance%5CCass.pdf","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Airline","Regulator":"FAA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00379d","key":"CFR","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00379d","_rev":"1-f0af0e5eeaf740024bbb74ff42f4a196","Acronym":"CFR","Name":"Code of Federal Regulations","Description":"The Code of Federal Regulations (CFR) is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government. It is divided into 50 titles that represent broad areas subject to Federal regulation. Each volume of the CFR is updated once each calendar year and is issued on a quarterly basis.","Link1":"CFR Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.gpoaccess.gov/cfr/index.html","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"All","Regulator":""}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd015191","key":"cGMP","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd015191","_rev":"1-d3bf1c96f91c3f58fc9f8332235fff9c","Acronym":"cGMP","Name":"Pharmaceutical Current Good Manufacturing Practices Initiative","Description":"On February 20, 2003, the Food and Drug Administration (FDA) released its first progress report on a major initiative concerning the regulation of drug product quality. The 2-year initiative, Pharmaceutical cGMPs for the 21st Century: A Risk-Based Approach (the Pharmaceutical cGMP initiative), which was launched on August 21, 2002, applies to human drug and biological drug products and veterinary drugs.","Link1":"cGMP Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.fda.gov/Drugs/DevelopmentApprovalProcess/Manufacturing/QuestionsandAnswersonCurrentGoodManufacturingPracticescGMPforDrugs/UCM071836","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Pharma","Regulator":"FDA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd006123","key":"COBIT","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd006123","_rev":"1-83bcff1e39e6d448b8d71e72d6e3bb2d","Acronym":"COBIT","Name":"Control Objectives for Information and related Technology","Description":"COBIT is a set of best practices (framework) for information technology (IT) management, created by the Information Systems Audit and Control Association (ISACA) and the IT Governance Institute (ITGI) in 1996. COBIT provides managers, auditors, and IT users with a set of generally accepted measures, indicators, processes and best practices, to assist them in maximizing the benefits derived through the use of information technology, and developing appropriate IT governance and control in a company.","Link1":"ISACA COBIT Site","Link2":"Comparison with IITL","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.isaca.org/Knowledge-Center/COBIT/Pages/Overview.aspx","Link2URL":"http://www.itmanagementonline.com/Resources/Articles/COBIT_vs_ITIL.pdf","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"All","Regulator":"ISACA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00cd25","key":"Dodd-Frank ","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00cd25","_rev":"3-3105e06895a33a41846f0a32d83ae0e3","Acronym":"Dodd-Frank ","Name":"Dodd-Frank Wall Street Reform and Consumer Protection Act","Description":"The Act, which was passed as a response to the late-2000s recession, is the most sweeping change to financial regulation in the United States since the Great Depression, and represents a paradigm shift in the American financial regulatory environment affecting all Federal financial regulatory agencies and affecting almost every aspect of the nation's financial services industry.","Link1":"Wikipedia","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://en.wikipedia.org/wiki/Dodd%E2%80%93Frank_Wall_Street_Reform_and_Consumer_Protection_Act","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Financial","Regulator":"US Congress"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd005c39","key":"EHS","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd005c39","_rev":"1-42a9f0e7a453f1ff73a3afa0de846a1d","Acronym":"EHS","Name":"World Bank Group Environmental, Health, and Safety Guidelines ","Description":"The EHS Guidelines are technical reference documents with general and industry-specific examples of Good International Industry Practice (GIIP), as defined in IFC's Performance Standard 3 on Pollution Prevention and Abatement. Reference to the EHS Guidelines by IFC clients is required under Performance Standard 3. IFC uses the EHS Guidelines as a technical source of information during project appraisal activities, as described in IFC's Environmental and Social Review Procedure.","Link1":"EHS Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.ifc.org/ifcext/sustainability.nsf/Content/EHSGuidelines","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"All","Regulator":"IFC"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00245f","key":"EPI","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00245f","_rev":"1-9f45eb952aa0fc3c7f6368dfed8edd1d","Acronym":"EPI","Name":"Element Performance Inspection","Description":"Type of inspection for ATOS surveillance.  Performance assessment confirming that an air carrier’s operating systems produce intended results, including mitigation or control of hazards and associated risks.  Conducted at the \"element\" level, but are accomplished by individual inspectors to determine if the carrier's system element processes meet established performance requirements, if the air carrier's procedures and controls are adhered to, and if proper records are maintained.","Link1":"EPI Database","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://fsims.faa.gov/PICResults.aspx?mode=Publication&doctype=EPI","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Airline","Regulator":"FAA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd012573","key":"EU Vigilance Reporting","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd012573","_rev":"1-f41c9e26d19d0c40fbeff0876569caf2","Acronym":"EU Vigilance Reporting","Name":"Guidelines On A Medical Devices Vigilance System","Description":"These guidelines cover the actions to be taken once the MANUFACTURER or National \nCompetent Authority receives information concerning an INCIDENT involving a MEDICAL \nDEVICE. Information on INCIDENTs which should be reported under the Medical Device \nVigilance System may come to the attention of MANUFACTURERs via the systematic \nprocedure to review experience gained from devices in the post-production phase, or by \nother means.","Link1":"EU Vigilance Reporting Document","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://ec.europa.eu/consumers/sectors/medical-devices/files/meddev/2_12_1-rev_6-12-2009_en.pdf","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Medical Device","Regulator":"EC"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd002ba6","key":"FAR","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd002ba6","_rev":"1-8b5fbbf03cbc1e2c7d902a1cc96ddd51","Acronym":"FAR","Name":"Federal Aviation Regulations","Description":"The Federal Aviation Regulations, or FARs, are rules prescribed by the Federal Aviation Administration (FAA) governing all aviation activities in the United States. The FARs are part of Title 14 of the Code of Federal Regulations (CFR). A wide variety of activities are regulated, such as airplane design, typical airline flights, pilot training activities, hot-air ballooning, lighter-than-air aircraft, man-made structure heights, obstruction lighting and marking, and even model rocket launches and model aircraft operation. The rules are designed to promote safe aviation, protecting pilots, flight attendants, passengers and the general public from unnecessary risk. They are also intended to protect the national security of the United States, especially in light of the September 11, 2001 attacks.","Link1":"FAR Database","Link2":"Wikipedia","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.airweb.faa.gov/Regulatory_and_Guidance_Library/rgFAR.nsf/MainFrame?OpenFrameSet","Link2URL":"http://en.wikipedia.org/wiki/Federal_Aviation_Regulations","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Airline","Regulator":"FAA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00eae1","key":"FDA Compliance","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00eae1","_rev":"1-f434af6d4cb9d73aee5f85f814ebbe28","Acronym":"FDA Compliance","Name":"FDA Food Compliance Programs","Description":"FDA's Compliance Programs provide instructions to FDA personnel for conducting activities to evaluate industry compliance with the Federal Food, Drug, and Cosmetic Act and other laws administered by FDA. Compliance Programs are made available to the public under the Freedom of Information Act. Compliance Programs do not create or confer any rights for or on any person and do not operate to bind FDA or the public. An alternative approach may be used as long as the approach satisfies the requirements of the applicable statutes and regulations.","Link1":"FDA Compliance Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.fda.gov/Food/GuidanceComplianceRegulatoryInformation/ComplianceEnforcement/ucm071496.htm","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Food and Safety","Regulator":"FDA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00b137","key":"FERC","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00b137","_rev":"1-3670b729a4035d61a41c66bbca9fdb07","Acronym":"FERC","Name":"Federal Energy Regulatory Commission","Description":"The Federal Energy Regulatory Commission, or FERC, is an independent agency that regulates the interstate transmission of electricity, natural gas, and oil. FERC also reviews proposals to build liquefied natural gas (LNG) terminals and interstate natural gas pipelines as well as licensing hydropower projects. The Energy Policy Act of 2005 gave FERC additional responsibilities as outlined in FERC's Top Initiatives and updated Strategic Plan.","Link1":"FERC Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.ferc.gov/default.asp","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Energy","Regulator":""}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd009a29","key":"FERPA","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd009a29","_rev":"1-67fbf541c7decfd1c8956c86b274cfbe","Acronym":"FERPA","Name":"Family Educational Rights and Privacy Act","Description":"The Family Educational Rights and Privacy Act (FERPA) (20 U.S.C. § 1232g; 34 CFR Part 99) is a Federal law that protects the privacy of student education records. The law applies to all schools that receive funds under an applicable program of the U.S. Department of Education.","Link1":"FERPA Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www2.ed.gov/policy/gen/guid/fpco/ferpa/index.html","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Educational","Regulator":"FPCO"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd007e1e","key":"FISMA","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd007e1e","_rev":"1-33ec14053f88a9742d57a64c3a53e3f4","Acronym":"FISMA","Name":"Federal Information Security Management Act","Description":"To promote the development of key security standards and guidelines to support the implementation of and compliance with the Federal Information Security Management Act including: ","Link1":"NIST / FISMA Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://csrc.nist.gov/groups/SMA/fisma/index.html","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"All","Regulator":"NIST"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd01096c","key":"FSIS","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd01096c","_rev":"1-d3c3c3f4f76d14d48989372b3bb32455","Acronym":"FSIS","Name":"Food Safety and Inspection Service","Description":"The Food Safety and Inspection Service (FSIS) is the public health agency in the U.S. Department of Agriculture responsible for ensuring that the nation's commercial supply of meat, poultry, and egg products is safe, wholesome, and correctly labeled and packaged.","Link1":"FSIS Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.fsis.usda.gov/about/index.asp","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Food and Safety","Regulator":"USDA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd015fab","key":"GCP","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd015fab","_rev":"1-025de95d4f454126e276935fcafb17fd","Acronym":"GCP","Name":"Guideline for Good Clinical Practice","Description":"Good Clinical Practice (GCP) is an international ethical and scientific quality \nstandard for designing, conducting, recording and reporting trials that involve the \nparticipation of human subjects. Compliance with this standard provides public \nassurance that the rights, safety and well-being of trial subjects are protected, \nconsistent with the principles that have their origin in the Declaration of Helsinki, \nand that the clinical trial data are credible.","Link1":"GCP Document","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Efficacy/E6_R1/Step4/E6_R1__Guideline.pdf","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Pharma","Regulator":"ICH"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00d9df","key":"GLB","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00d9df","_rev":"1-afb085f5411b90ad233bb0c02ce37080","Acronym":"GLB","Name":"Gramm–Leach–Bliley Act","Description":"The Gramm–Leach–Bliley Act repealed part of the Glass–Steagall Act of 1933, opening up the market among banking companies, securities companies and insurance companies. The Glass–Steagall Act prohibited any one institution from acting as any combination of an investment bank, a commercial bank, and an insurance company.","Link1":"Wikipedia","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://en.wikipedia.org/wiki/Gramm%E2%80%93Leach%E2%80%93Bliley_Act","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Financial","Regulator":"US Congress"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd016d09","key":"GLP","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd016d09","_rev":"1-6d6b58357a3c611e88a2eee0a16820b9","Acronym":"GLP","Name":"Principles of Good Laboratory Practice","Description":"The primary objective of the OECD Principles of Good Laboratory Practice (GLP) is to ensure the generation of high quality and reliable test data related to the safety of industrial chemical substances and preparations in the framework of harmonising testing procedures for the Mutual Acceptance of Data (MAD).","Link1":"GLP Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.oecd.org/department/0,3355,en_2649_34381_1_1_1_1_1,00.html","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Pharma","Regulator":"OECD"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00dfe2","key":"Gramm-Leach-Bliley","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00dfe2","_rev":"1-02f77ddba45985a2961731575be89a6b","Acronym":"Gramm-Leach-Bliley","Name":"Gramm-Leach-Bliley Act (GLBA)","Description":"The Gramm–Leach–Bliley Act allowed commercial banks, investment banks, securities firms, and insurance companies to consolidate","Link1":"Wikipedia","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://en.wikipedia.org/wiki/Gramm%E2%80%93Leach%E2%80%93Bliley_Act","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Financial","Regulator":"US Congress"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00f894","key":"HACCP","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00f894","_rev":"1-814f81de614364fa6a456ab9da3faee7","Acronym":"HACCP","Name":"Hazard Analysis & Critical Control Points","Description":"HACCP is a management system in which food safety is addressed through the analysis and control of biological, chemical, and physical hazards from raw material production, procurement and handling, to manufacturing, distribution and consumption of the finished product.","Link1":"HACCP Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.fda.gov/food/foodsafety/hazardanalysiscriticalcontrolpointshaccp/default.htm","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Food and Safety","Regulator":"FDA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00a1fb","key":"HEOA","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00a1fb","_rev":"1-70107b428902a40bc570fc4fa266d211","Acronym":"HEOA","Name":"Higher Education Opportunity Act","Description":"The Higher Education Opportunity Act (Public Law 110-315) (HEOA) was enacted on August 14, 2008, and reauthorizes the Higher Education Act of 1965, as amended (the HEA). The HEOA makes a number of changes to programs authorized under the HEA, authorizes new programs, and makes changes to other laws.","Link1":"HEOA Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www2.ed.gov/policy/highered/leg/hea08/index.html","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Educational","Regulator":"US Congress"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd010f7c","key":"HIPAA","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd010f7c","_rev":"1-87f14cf39104e324308ad6364831a79b","Acronym":"HIPAA","Name":"Health Insurance Portability and Accountability Act","Description":"The Health Insurance Portability and Accountability Act (HIPAA) of 1996 protects health insurance coverage for workers and their families when they change or lose their jobs. Title II of HIPAA, known as the Administrative Simplification (AS) provisions, requires the establishment of national standards for electronic health care transactions and national identifiers for providers, health insurance plans, and employers.","Link1":"Wikipedia","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://en.wikipedia.org/wiki/Health_Insurance_Portability_and_Accountability_Act","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Healthcare","Regulator":"US Congress"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd011ce5","key":"HITECH Act","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd011ce5","_rev":"1-e95ad8ce175b7b37d2a4f9557223e9cb","Acronym":"HITECH Act","Name":"Health Information Technology for Economic and Clinical Health Act","Description":"The Health Information Technology for Economic and Clinical Health (HITECH) Act, enacted as part of the American Recovery and Reinvestment Act of 2009, was signed into law on February 17, 2009, to promote the adoption and meaningful use of health information technology.  Subtitle D of the HITECH Act addresses the privacy and security concerns associated with the electronic transmission of health information, in part, through several provisions that strengthen the civil and criminal enforcement of the HIPAA rules.  ","Link1":"HITECH Act Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.hhs.gov/ocr/privacy/hipaa/administrative/enforcementrule/hitechenforcementifr.html","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Healthcare","Regulator":"US Congress"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd0043ba","key":"ISACA","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd0043ba","_rev":"1-e54ced5f283a05fd854351b34c3d15a9","Acronym":"ISACA","Name":"Information Systems Audit and Control Association","Description":"A nonprofit, independent membership association, ISACA is a leading global provider of knowledge, certifications, community, advocacy and education on information systems assurance, control and security, enterprise governance of IT, and IT-related risk and compliance. Founded in 1969 as the EDP Auditors Association, ISACA helps its members and their employers ensure trust in, and value from, information systems.","Link1":"ISACA Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"https://www.isaca.org/Pages/default.aspx","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"All","Regulator":""}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd013584","key":"ISO 13485","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd013584","_rev":"1-974e52fd3ebf606ac836faa282be8047","Acronym":"ISO 13485","Name":"ISO Standards for Medical devices -- Quality management systems -- Requirements for regulatory purposes","Description":"ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.","Link1":"ISO 13485 Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.iso.org/iso/catalogue_detail?csnumber=36786","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Medical Device","Regulator":"ISO"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00fa08","key":"ISO 22000","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00fa08","_rev":"1-62a9ef461ea83ee2884bc7a5da042775","Acronym":"ISO 22000","Name":"ISO Standards for Food safety management systems -- Requirements for any organization in the food chain","Description":"ISO 22000:2005 specifies requirements for a food safety management system where an organization in the food chain needs to demonstrate its ability to control food safety hazards in order to ensure that food is safe at the time of human consumption.","Link1":"ISO 22000 Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.iso.org/iso/catalogue_detail?csnumber=35466","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Food and Safety","Regulator":"ISO"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd006d91","key":"ISO 31000","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd006d91","_rev":"1-fb6f7b74c64da2afe4a583846b1a2c05","Acronym":"ISO 31000","Name":"ISO Standards for Risk Management","Description":"The purpose of ISO 31000:2009 is to provide principles and generic guidelines on risk management.","Link1":"Wikipedia","Link2":"ISO Site","Link3":"","Link4":"","Link5":"","Link1URL":"http://en.wikipedia.org/wiki/ISO_31000","Link2URL":"http://www.iso.org/iso/catalogue_detail.htm?csnumber=43170","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"All","Regulator":"ISO"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd0123de","key":"ISO 9000","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd0123de","_rev":"1-c657328412cbaba3ed49dd26dcedea0d","Acronym":"ISO 9000","Name":"ISO Standards for Quality Management","Description":"The ISO 9000 family of standards represents an international consensus on good quality management practices. It consists of standards and guidelines relating to quality management systems and related supporting standards.","Link1":"ISO 9000 Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.iso.org/iso/iso_9000_essentials","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Hi-Tech Manufacturing","Regulator":"ISO"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00740f","key":"ISO/IEC 27000","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00740f","_rev":"1-bbf31fd0469bb7fc616d63b08fa4d5fa","Acronym":"ISO/IEC 27000","Name":"Information Security Standard","Description":"The ISO/IEC 27000-series (also known as the 'ISMS Family of Standards' or 'ISO27k' for short) provides best practice recommendations on information security management, risks and controls within the context of an overall Information Security Management System (ISMS), similar in design to management systems for quality assurance (the ISO 9000 series) and environmental protection (the ISO 14000 series).","Link1":"Wikipedia","Link2":"ISO/IEC 27002 Site","Link3":"","Link4":"","Link5":"","Link1URL":"http://en.wikipedia.org/wiki/ISO/IEC_27000-series","Link2URL":"http://www.iso27001security.com/html/27002.html","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"All","Regulator":"ISO/IEC"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd008ab9","key":"ITIL","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd008ab9","_rev":"1-2df1ec48fe696d15efcfc0f041cfb6d7","Acronym":"ITIL","Name":"Information Infrastructure  Library","Description":"ITIL® is the most widely adopted approach for IT Service Management in the world.  It provides a practical, no-nonsense framework for identifying, planning, delivering and supporting IT services to the business.  \nThe Information Technology Infrastructure Library (ITIL) is a set of concepts and practices for Information Technology Services Management (ITSM), Information Technology (IT) development and IT operations.\nITIL gives detailed descriptions of a number of important IT practices and provides comprehensive checklists, tasks and procedures that any IT organization can tailor to its needs. ITIL is published in a series of books, each of which covers an IT management topic. The names ITIL and IT Infrastructure Library are registered trademarks of the United Kingdom's Office of Government Commerce (OGC).","Link1":"ITIL Site","Link2":"ITIL Glossary","Link3":"ITIL Acronyms","Link4":"Wikipedia","Link5":"Comparison with COBIT","Link1URL":"http://www.itil-officialsite.com/home/home.aspx","Link2URL":"http://www.itil-officialsite.com/nmsruntime/saveasdialog.asp?lID=910&sID=242","Link3URL":"http://www.itil-officialsite.com/nmsruntime/saveasdialog.asp?lID=903&sID=242","Link4URL":"http://en.wikipedia.org/wiki/Information_Technology_Infrastructure_Library#9._Small-Scale_Implementation","Link5URL":"http://www.itmanagementonline.com/Resources/Articles/COBIT_vs_ITIL.pdf","Industry":"All","Regulator":"OGC"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd012ee0","key":"MedWatch","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd012ee0","_rev":"1-8bd8efe99f113e921651c8df51b5ed98","Acronym":"MedWatch","Name":"FDA MedWatch Reporting","Description":"The FDA Safety Information and Adverse Event Reporting Program.  Clinically important medical product safety alerts.","Link1":"MedWatch Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.fda.gov/Safety/MedWatch/default.htm","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Medical Device","Regulator":"FDA"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00b911","key":"NERC","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00b911","_rev":"1-e48a0a7d6663bb8e190eb96a8046bbe7","Acronym":"NERC","Name":"North American Electric Reliability Corporation","Description":"The North American Electric Reliability Corporation’s (NERC) mission is to ensure the reliability of the North American bulk power system. NERC is the electric reliability organization (ERO) certified by the Federal Energy Regulatory Commission to establish and enforce reliability standards for the bulk-power system. NERC develops and enforces reliability standards; assesses adequacy annually via a 10-year forecast, and summer and winter forecasts; monitors the bulk power system; and educates, trains and certifies industry personnel. ERO activities in Canada related to the reliability of the bulk-power system are recognized and overseen by the appropriate governmental authorities in that country.","Link1":"NERC Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.nerc.com/index.php","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Energy","Regulator":""}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00c730","key":"OMB A-123","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00c730","_rev":"1-8ddb0be9005383b40cb1b5175963c681","Acronym":"OMB A-123","Name":"OMB Circular A-123, Management’s Responsibility for Internal \nControl","Description":"OMB Circular No. A-123 defines management's responsibility for internal control in Federal \nagencies. A re-examination of the existing internal control requirements for Federal agencies \nwas initiated in light of the new internal control requirements for publicly-traded companies \ncontained in the Sarbanes-Oxley Act of 2002. Circular A-123 and the statute it implements, the \nFederal Managers’ Financial Integrity Act of 1982, are at the center of the existing Federal \nrequirements to improve internal control.","Link1":"OMB A-123 Document","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.whitehouse.gov/sites/default/files/omb/assets/omb/circulars/a123/a123_rev.pdf","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Financial","Regulator":"OMB"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd005096","key":"OSHA","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd005096","_rev":"1-bf40fabfd0928cfc092be5172930a87b","Acronym":"OSHA","Name":"Occupational Safety & Health Administration","Description":"OSHA standards are rules that describe the methods employers are legally required to follow to protect their workers from hazards. Before OSHA can issue a standard, it must go through a very extensive and lengthy process that includes substantial public engagement, notice and comment. The agency must show that a significant risk to workers exists and that there are feasible measures employers can take to protect their workers.","Link1":"OSHA Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.osha.gov/","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"All","Regulator":""}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd016bfe","key":"Q7A","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd016bfe","_rev":"1-e385ddb48817f392293e7a128c38be7e","Acronym":"Q7A","Name":"Q7A Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients","Description":"This document is intended to provide guidance regarding good manufacturing practice (GMP) for the manufacturing of active pharmaceutical ingredients (APIs) under an appropriate system for managing quality.  It is also intended to help ensure that APIs meet the quality and purity characteristics that they purport, or are represented, to possess.","Link1":"Q7A Document","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.fda.gov/downloads/RegulatoryInformation/Guidances/ucm129098.pdf","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Pharma","Regulator":"ICH"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd00bd43","key":"Regulation CC","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd00bd43","_rev":"1-e11cd71278094c868c508bf83849e88b","Acronym":"Regulation CC","Name":"Availability of Funds and Collection of Checks","Description":"Governs the availability of funds deposited in checking accounts and the collection and return of checks","Link1":"Regulation CC Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.federalreserve.gov/bankinforeg/reglisting.htm#CC","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Financial","Regulator":"FRB"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd009113","key":"SOX","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd009113","_rev":"1-b88c635e1dbe30df145cc0d95c943982","Acronym":"SOX","Name":"Sarbanes-Oxley Act of 2002","Description":"The Sarbanes–Oxley Act of 2002 is a United States federal law enacted on July 30, 2002, which set new or enhanced standards for all U.S. public company boards, management and public accounting firms. ","Link1":"Wikipedia","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://en.wikipedia.org/wiki/Sarbanes%E2%80%93Oxley_Act","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"All","Regulator":"US Congress"}},
{"id":"1d9fbe912b5b2f43f5c9bcd3dd0109d7","key":"TJC","value":{"_id":"1d9fbe912b5b2f43f5c9bcd3dd0109d7","_rev":"1-abd498fff74d4a43aff1fedc32e82b54","Acronym":"TJC","Name":"The Joint Commission","Description":"Formerly JCAHO, TJC is an independent, not-for-profit organization that accredits and certifies more than 19,000 health care organizations and programs in the United States. Joint Commission accreditation and certification is recognized nationwide as a symbol of quality that reflects an organization’s commitment to meeting certain performance standards.","Link1":"TJC Site","Link2":"","Link3":"","Link4":"","Link5":"","Link1URL":"http://www.jointcommission.org/","Link2URL":"","Link3URL":"","Link4URL":"","Link5URL":"","Industry":"Healthcare","Regulator":""}}
]}