82 relations: Accounting, Accreditation, Accuracy and precision, Agilent Technologies, Agriculture, Aircraft, Analytical balance, Analytical chemistry, Application software, Assay, Authentication, Barry Boehm, BIOS, Bridge, British Pharmacopoeia, Building, Certification of voting machines, Change control, Civil engineering, Clinical trial, Common Criteria, Comparability, Cross-validation, Cross-validation (analytical chemistry), Curve fitting, Department of Health (United Kingdom), Depreciation, Detection limit, Do it yourself, Economics, Elsevier, European Pharmacopoeia, Fatigue (material), Fault tolerance, Food, Food and Drug Administration, Formal verification, Functional verification, Good Automated Manufacturing Practice, Good laboratory practice, Greenhouse gas, GUID Partition Table, GxP, Health Canada, Health care, Health Sciences Authority, INI file, Institute of Electrical and Electronics Engineers, Integrity testing, International Organization for Standardization, ..., ISO 9000, ISO/IEC 17025, ISO/IEC 27001:2013, John Wiley & Sons, Medical device, Medicine, Monograph, Pharmaceutical drug, Population, Project Management Body of Knowledge, Quality management system, Real estate appraisal, Repeatability, Reproducibility, Requirement, Road, Road safety audit, Software, Software verification and validation, Specification (technical standard), System testing, Systematic political science, The International Pharmacopoeia, Third-party verification, Title 21 of the Code of Federal Regulations, United States Department of Health and Human Services, United States Pharmacopeia, Usability testing, Vehicle inspection, Verification and validation of computer simulation models, Wiley-VCH, Windows Registry. Expand index (32 more) » « Shrink index
Accounting or Accountancy is the measurement, processing and communication of financial information about economic entities.
Accreditation is the process in which certification of competency, authority, or credibility is presented.
Accuracy and precision are defined in terms of systematic and random errors.
Agilent Technologies is an American public research, development and manufacturing company established in 1999 as a spin-off from Hewlett Packard.
Agriculture is the cultivation of animals, plants, fungi, and other life forms for food, fiber, biofuel, medicinal and other products used to sustain and enhance human life.
An aircraft is a machine that is able to fly by gaining support from the air, or, in general, the atmosphere of a planet.
An analytical balance (often called a "lab balance") is a class of balance designed to measure small mass in the sub-milligram range.
Analytical chemistry is the study of the separation, identification, and quantification of the chemical components of natural and artificial materials.
An application program (or application for short) is a computer program designed to perform a group of coordinated functions, tasks, or activities for the benefit of the user.
An assay is an investigative (analytic) procedure in laboratory medicine, pharmacology, environmental biology and molecular biology for qualitatively assessing or quantitatively measuring the presence or amount or the functional activity of a target entity (the analyte).
Authentication (from authentikos, "real, genuine," from αὐθέντης authentes, "author") is the act of confirming the truth of an attribute of a single piece of data (a datum) claimed true by an entity.
Barry W. Boehm (born 1935) is an American software engineer, Distinguished Professor http://about.usc.edu/faculty/distinguished-professors/ of Computer Science, Industrial and Systems Engineering; the TRW Professor of Software Engineering; and Founding Director of the Center for Systems and Software Engineering at the University of Southern California.
The BIOS (an acronym for Basic Input/Output System and also known as the System BIOS, ROM BIOS or PC BIOS) is a type of firmware used to perform hardware initialization during the booting process (power-on startup) on IBM PC compatible computers, and to provide runtime services for operating systems and programs.
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A bridge is a structure built to span physical obstacles such as a body of water, valley, or road, for the purpose of providing passage over the obstacle.
The British Pharmacopoeia (BP) is an annual published collection of quality standards for UK medicinal substances.
A building or edifice is a man-made structure with a roof and walls standing more or less permanently in one place, such as a house or factory.
Various governments require a certification of voting machines.
Change control within quality management systems (QMS) and information technology (IT) systems is a formal process used to ensure that changes to a product or system are introduced in a controlled and coordinated manner.
Civil engineering is a professional engineering discipline that deals with the design, construction, and maintenance of the physical and naturally built environment, including works like roads, bridges, canals, dams, and buildings.
Clinical trials are experiments done in clinical research.
The Common Criteria for Information Technology Security Evaluation (abbreviated as Common Criteria or CC) is an international standard (ISO/IEC 15408) for computer security certification.
In mathematics, any two elements x and y of a set P that is partially ordered by a binary relation ≤ are comparable when either x ≤ y or y ≤ x. If it is not the case that x and y are comparable, then they are called incomparable.
Cross-validation could refer to.
Cross-validation is an approach by which the sets of scientific data generated using two or more methods are critically assessed.
Curve fitting is the process of constructing a curve, or mathematical function, that has the best fit to a series of data points, possibly subject to constraints.
The Department of Health (DH) is the Ministerial Department of the United Kingdom Government responsible for government policy on health and adult social care matters in England, along with a few elements of the same matters which are not otherwise devolved to the Scottish Government, Welsh Government or Northern Ireland Executive.
In accountancy, depreciation refers to two aspects of the same concept.
In analytical chemistry, the detection limit, lower limit of detection, or LOD (limit of detection), is the lowest quantity of a substance that can be distinguished from the absence of that substance (a blank value) within a stated confidence limit (generally 1%).
Do it yourself, also known as DIY, is the method of building, modifying, or repairing something without the aid of experts or professionals.
Economics is the social science that seeks to describe the factors which determine the production, distribution and consumption of goods and services.
Elsevier B.V. is an academic publishing company that publishes medical and scientific literature.
The European Pharmacopoeia (Pharmacopoea Europaea, Ph. Eur.) is a published collection of monographs that describe both the individual and general quality standards for ingredients, dosage forms and methods of analysis for medicines.
In materials science, fatigue is the weakening of a material caused by repeatedly applied loads.
Fault tolerance is the property that enables a system to continue operating properly in the event of the failure of (or one or more faults within) some of its components.
Food is any substance consumed to provide nutritional support for the body.
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The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments.
In the context of hardware and software systems, formal verification is the act of proving or disproving the correctness of intended algorithms underlying a system with respect to a certain formal specification or property, using formal methods of mathematics.
Functional verification, in electronic design automation, is the task of verifying that the logic design conforms to specification.
Good Automated Manufacturing Practice (GAMP) is both a technical subcommittee of the International Society for Pharmaceutical Engineering (ISPE) and a set of guidelines for manufacturers and users of automated systems in the pharmaceutical industry.
In the experimental (non-clinical) research arena, the phrase good laboratory practice or GLP specifically refers to a quality system of management controls for research laboratories and organizations to try to ensure the uniformity, consistency, reliability, reproducibility, quality, and integrity of chemical (including pharmaceuticals) non-clinical safety tests; from physio-chemical properties through acute to chronic toxicity tests.
A greenhouse gas (sometimes abbreviated GHG) is a gas in an atmosphere that absorbs and emits radiation within the thermal infrared range.
GUID Partition Table (GPT) is a standard for the layout of the partition table on a physical hard disk, using globally unique identifiers (GUID).
GxP is a general term for Good (Anything...) Practice quality guidelines and regulations.
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Health Canada (French: Santé Canada) is the department of the government of Canada with responsibility for national public health.
Health care or healthcare is the diagnosis, treatment, and prevention of disease, illness, injury, and other physical and mental impairments in human beings.
The Health Sciences Authority (Abbreviation: HSA; Chinese: 卫生科学局); Malay: Penguasa Sains Kesihatan) is a statutory board under the Ministry of Health of the Singapore Government.
The INI file format is an informal standard for configuration files for some platforms or software.
The Institute of Electrical and Electronics Engineers (IEEE) is a professional association with its corporate office in New York City and its operations center in Piscataway, New Jersey.
Integrity testing may refer to.
The International Organization for Standardization (ISO) is an international standard-setting body composed of representatives from various national standards organizations.
The ISO 9000 family of quality management systems standards is designed to help organizations ensure that they meet the needs of customers and other stakeholders while meeting statutory and regulatory requirements related to a product.
ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories is the main ISO standard used by testing and calibration laboratories.
ISO 27001:2013 is an information security standard that was published on the 25th September 2013.
John Wiley & Sons, Inc., also referred to as Wiley, is a global publishing company that specializes in academic publishing and markets its products to professionals and consumers, students and instructors in higher education, and researchers and practitioners in scientific, technical, medical, and scholarly fields.
A medical device is an instrument, apparatus, implant, in vitro reagent, or similar or related article that is used to diagnose, prevent, or treat disease or other conditions, and does not achieve its purposes through chemical action within or on the body (which would make it a drug).
Medicine (British English; American English) is the science and practice of the diagnosis, treatment, and prevention of disease.
A monograph is a specialist work of writing (in contrast to reference works) on a single subject or an aspect of a subject, usually by a single author.
A pharmaceutical drug (also referred to as a medicinal product, medicine, medication, or medicament) is a drug used to diagnose, cure, treat, or prevent disease.
A population is a summation of all the organisms of the same group or species, which live in a particular geographical area, and have the capability of interbreeding.
A Guide to the Project Management Body of Knowledge (PMBOK Guide) is a book which presents a set of standard terminology and guidelines (a body of knowledge) for project management.
A quality management system (QMS) is a collection of business processes focused on achieving quality policy and quality objectives to meet customer requirements.
Real estate appraisal, property valuation or land valuation is the process of developing an opinion of value for real property (usually market value).
Repeatability or test–retest reliability is the variation in measurements taken by a single person or instrument on the same item, under the same conditions, and in a short period of time.
Reproducibility is the ability of an entire experiment or study to be duplicated, either by the same researcher or by someone else working independently.
In product development and process optimization, a requirement is a singular documented physical and functional need that a particular design, product or process must be able to perform.
A road is a thoroughfare, route, or way on land between two places that has been paved or otherwise improved to allow travel by some conveyance, including a horse, cart, bicycle, or motor vehicle.
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A Road Safety Audit (RSA) is defined as "the formal safety performance examination of an existing or future road or intersection by an independent, multidisciplinary team.
Computer software or simply software is any set of machine-readable instructions that directs a computer's processor to perform specific operations.
In software project management, software testing, and software engineering, verification and validation (V&V) is the process of checking that a software system meets specifications and that it fulfills its intended purpose.
There are different types of specifications, which generally are mostly types of documents, forms or orders or relates to information in databases.
System testing of software or hardware is testing conducted on a complete, integrated system to evaluate the system's compliance with its specified requirements.
Systematic political science, as developed by Dallas F. Bell Jr., basically is the use of game theory methods to mathematically unify the anthropocentric academic disciplines of theology, epistemology, psychology, sociology and eschatology for computerized analysis and predictions after verification and validation methods are employed, such as red team procedures.
The aim of The International Pharmacopoeia (Ph. Int.), which is issued by the World Health Organization as a recommendation, is to achieve a wide global uniformity of quality specifications for selected pharmaceutical products, excipients, and dosage forms.
Third party verification (TPV) is a process of getting an independent party to confirm that the customer is actually requesting a change or ordering a new service or product.
Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of National Drug Control Policy (ONDCP).
The United States Department of Health and Human Services (HHS), also known as the Health Department, is a cabinet-level department of the U.S. federal government with the goal of protecting the health of all Americans and providing essential human services.
The United States Pharmacopeia (USP) publishes an official compendium in a combined volume with the National Formulary as the USP-NF.
Usability testing is a technique used in user-centered interaction design to evaluate a product by testing it on users.
Vehicle inspection is a procedure mandated by national or subnational governments in many countries, in which a vehicle is inspected to ensure that it conforms to regulations governing safety, emissions, or both.
Verification and Validation of Computer Simulation Models is conducted during the development of a simulation model with the ultimate goal of producing an accurate and credible model.
Wiley-VCH is a German publisher owned by John Wiley & Sons.
Windows Registry is a hierarchical database that stores configuration settings and options on Microsoft Windows operating systems.
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