regulatory documentation

regulatory documentation
Банковское дело: регулятивные документы

Универсальный англо-русский словарь. . 2011.

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Смотреть что такое "regulatory documentation" в других словарях:

  • Documentation — is a term used in several different ways. Generally, documentation (to document) refers to the process of providing evidence. Modules of Documentation are Helpful. The most common meanings are: the process of documenting knowledge (or rather… …   Wikipedia

  • Requirements-driven product documentation development — Overview Requirement driven product documentation development is a documentation development process in which ongoing changes in a product s requirements cause ongoing changes in the product documentation throughout the product life cycle.… …   Wikipedia

  • ISA 230 Documentation — is one of the International Standards on Auditing. It serves to direct the documentation of audit working papers in order to assist the audit planning and performance; the supervision and review of the audit work; and the recording of audit… …   Wikipedia

  • Transportation Recall Enhancement, Accountability and Documentation Act — The Transportation Recall Enhancement, Accountability and Documentation (or TREAD) Act is a United States federal law enacted in the fall of 2000. This law intends to increase consumer safety through mandates assigned to the National Highway… …   Wikipedia

  • Submission management — Regulatory submissions in the pharmaceutical/biotechnology and medical device industry are comprised of documents and data that are submitted to a Regulatory Agency to gain approval to market new drugs, biologics and devices. The documentation… …   Wikipedia

  • Automated Tissue Image Systems — (ATIS) are computer controlled automatic test equipment (ATE) systems classified as medical device and used as pathology laboratory tools (tissue based cancer diagnostics) to characterize a stained tissue sample embedded on a bar coded glass… …   Wikipedia

  • Clinical trial — Clinical trials are a set of procedures in medical research and drug development that are conducted to allow safety (or more specifically, information about adverse drug reactions and adverse effects of other treatments) and efficacy data to be… …   Wikipedia

  • Subprime mortgage crisis — Part of a series on: Late 2000s financial crisis Major dimensions …   Wikipedia

  • EXL — Infobox Company company name = EXL Service Holdings, Inc. company company type = Multinational company slogan = Global Services. Value Delivered foundation = 1999 location = New York, US key people = Vikram Talwar, Executive Chairman; Noida,… …   Wikipedia

  • Medical writing — is the activity of producing scientific documentation by a specialized writer. The medical writer typically is not one of the scientists or doctors who performed the research. A medical writer, working with doctors, scientists, and other subject… …   Wikipedia

  • Validation (drug manufacture) — Within the highly regulated environment for development and manufacturing of Pharmaceutical Drugs and medical devices there is a requirement within the regulations to provide an appropriate amount of assurance that critical processes in producing …   Wikipedia


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