- Medical Devices Agency
- Медицина: Агентство по медицинским приборам, Агентство медицинских приборов
Универсальный англо-русский словарь. Академик.ру. 2011.
Medical Devices Agency
Смотреть что такое "Medical Devices Agency" в других словарях:
Pharmaceuticals and Medical Devices Agency — Die PMDA (jap. (独立行政法人)医薬品医療機器総合機構, (dokuritsu gyōsei hōjin) iyakuhin iryōkiki sōgō kikō; dt. „(Unabhängiges Verwaltungsorgan) Allgemeine Organisation für Pharmazeutika und medizinische Geräte“ engl. Pharmaceuticals and Medical Devices Agency)… … Deutsch Wikipedia
Medical Products Agency (Sweden) — The Medical Products Agency (Swedish: Läkemedelsverket) is the Swedish national authority responsible for regulation and surveillance of the development, manufacturing and sale of medicinal drugs, medical devices and cosmetics. Its task is also… … Wikipedia
European Medical Devices Industry Group — The European Medical Devices Industry Group (EMIG) is a non profit trade association, and represents the medical devices industry in Europe as defined by the European Union Medical Devices Directives (93/42/EEC). Karen Howes is the current chair… … Wikipedia
Medical translation — is the translation of technical, regulatory, clinical or marketing documentation, software or training curriculum for the pharmaceutical, medical device or healthcare fields. Most countries around the world require that literature and labeling… … Wikipedia
Medical Technology Assessment — (MTA) is the objective evaluation of a medical technology regarding its safety and performance, its (future) impact on clinical and non clinical patient outcomes as well as its interactive effects on economical, organizational, social, juridical… … Wikipedia
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
Medicines and Healthcare products Regulatory Agency — The logo of the MHRA. The Medicines and Healthcare products Regulatory Agency (MHRA) is the UK government agency which is responsible for ensuring that medicines and medical devices work and are acceptably safe. The agency was formed on 1 April… … Wikipedia
Medical Communications for Combat Casualty Care — (MC4) is a combat health support information management system of the U.S. Army. MC4 integrates, fields and supports medical (patient) information for tactical medical forces, enabling a comprehensive, lifelong electronic medical record for all… … Wikipedia
Medicines and Healthcare products Regulatory Agency — Die Medicines and Healthcare Products Regulatory Agency (MHRA) ist die medizinische Zulassungs und Aufsichtsbehörde für Arzneimittel in Großbritannien. Zu ihren Aufgaben gehört unter anderem der Betrieb eines Zulassungssystems für Medikamente vor … Deutsch Wikipedia
Medical prescription — ℞ redirects here. For other uses of Rx, see Rx. A prescription (℞) is a health care program implemented by a physician or other medical practitioner in the form of instructions that govern the plan of care for an individual patient.[1]… … Wikipedia
Medical error — A medical error may be defined as a preventable adverse effect of care, whether or not it is evident or harmful to the patient. This might include an inaccurate or incomplete diagnosis or treatment of a disease, injury, syndrome, behavior,… … Wikipedia
