Перевод: с русского на все языки

со всех языков на русский

(In-Vitro Diagnostic Device)

См. также в других словарях:

  • Medical device — A medical device is a product which is used for medical purposes in patients, in diagnosis, therapy or surgery[citation needed]. Whereas medicinal products (also called pharmaceuticals) achieve their principal action by pharmacological, metabolic …   Wikipedia

  • Promega — History and Background =In 1978 scientists were just beginning to understand the potential of what Boyer and Cohen had done by cutting DNA into specific fragments using restriction enzymes, rejoining them and transferring them into bacterial host …   Wikipedia

  • Stool guaiac test — It involves feces, a thick piece of paper attached to a thin film coated with guaiac (which comes from the Guaiacum tree [cite web | url = http://www.fda.gov/cdrh/oivd/guidance/772.html#5a | title = Guidance for Industry and FDA Staff Review… …   Wikipedia

  • Food and Drug Administration — FDA redirects here. For other uses, see FDA (disambiguation). Food and Drug Administration Agency overview Formed 1906 …   Wikipedia

  • IVD — interactive videodisk; intervertebral disc; in vitro diagnostic device …   Medical dictionary

  • IVD — • interactive videodisk; • intervertebral disc; • in vitro diagnostic device …   Dictionary of medical acronyms & abbreviations

  • Mindray Medical International Limited — Type Public (NYSE: MR) Industry Medical Devices …   Wikipedia

  • China Medical Technologies — Inc. Type Public (NASDAQ:CMED) Industry Medical technology Founded …   Wikipedia

  • List of IEC standards — In order to distinguish standards published by the International Electrotechnical Commission numerically from other international standards, their number range was shifted in 1997 by adding 60000. So what used to be called IEC 27 is now… …   Wikipedia

  • ISO 13485 — is an ISO standard, published in 2003, that represents the requirements for a comprehensive management system for the design and manufacture of medical devices. This standard supersedes earlier documents such as EN 46001 and EN 46002 (both 1997) …   Wikipedia

  • Verification and Validation — Verification Validation is the process of checking that a product, service, or system meets specifications and that it fulfils its intended purpose. These are critical components of a quality management system such as ISO… …   Wikipedia

Поделиться ссылкой на выделенное

Прямая ссылка:
Нажмите правой клавишей мыши и выберите «Копировать ссылку»