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Adverse Event Reporting System

См. также в других словарях:

  • Vaccine Adverse Event Reporting System — The Vaccine Adverse Event Reporting System is a United States program for vaccine safety, co sponsored by the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA). VAERS is a post marketing safety… …   Wikipedia

  • Critical Incident Reporting System — Ein Critical Incident Reporting System (CIRS) (eng. Berichtssystem für kritische Zwischenfälle) ist ein Berichtssystem zur anonymen Meldung von kritischen Ereignissen (critical incident) und Beinahe Schäden (near miss) in Einrichtungen des… …   Deutsch Wikipedia

  • Adverse effect — Classification and external resources ICD 10 T78 ICD 9 995.89 In medicine, an …   Wikipedia

  • Adverse effect (medicine) — In medicine, an adverse effect is a harmful and undesired effect resulting from a medication or other intervention such as chemotherapy or surgery. An adverse effect may be termed a side effect (when judged to be secondary to a main or… …   Wikipedia

  • Adverse drug reaction — Classification and external resources Adverse drug reaction leading to hepatitis (drug induced hepatitis) with granulomata. Other causes were excluded with extensive investigations. Liver biopsy …   Wikipedia

  • Clinical Trial Management System — Ein klinisches Studienmanagementsystem (Clinical Trial Management System; CTMS) ist eine Softwarekategorie, die in der Biotechnologie und Pharmaindustrie angewendet wird, um das Management von klinischen Studien zu unterstützen. Mit Hilfe eines… …   Deutsch Wikipedia

  • Clinical Trial Management System — A Clinical Trial Management System, also known as CTMS , is a customizeable software system used by the biotechnology and pharmaceutical industries to manage the large amounts of data involved with the operation of a clinical trial. It maintains… …   Wikipedia

  • Clinical trial management system — A Clinical Trial Management System, also known as CTMS, is a customizable software system used by the biotechnology and pharmaceutical industries to manage the large amounts of data involved with the operation of a clinical trial. It maintains… …   Wikipedia

  • Quality Controlled Trial Management System — Ein Qualitätskontrolliertes Studienmanagementsystem (Quality Controlled Trial Management System; QCTMS) gehört zur Softwarekategorie Clinical Trial Management System (CTMS), die in der Medizinprodukte , Biotechnologie und Pharmaindustrie… …   Deutsch Wikipedia

  • Research on Adverse Drug events And Reports — (RADAR) is a pharmacovigilance team of 25 doctors who receive calls about possible adverse drug reactions and investigate. RADAR is based out of Northwestern s Feinberg School of Medicine and the VA Center for Management of Complex Chronic Care… …   Wikipedia

  • Radar (Research on Adverse Drug events And Reports) — The aims of the Research on Adverse Drug events And Reports (RADAR) Project are to disseminate safety reports for serious adverse drug reactions (sADRs) and to identify barriers to identification and reporting of these clinical events.… …   Wikipedia

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