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Food and Drug Administration — FDA redirects here. For other uses, see FDA (disambiguation). Food and Drug Administration Agency overview Formed 1906 … Wikipedia
Bisphosphonate — Basic structure of a bisphosphonate on top. To compare the structure of pyrophosphate below. Note the similarity in structure. Bisphosphonates (also called diphosphonates) are a class of drugs that prevent the loss of bone mass, used to treat… … Wikipedia
Biomedical engineering — For the Russian journal on the subject, see Meditsinskaya Tekhnika. Ultrasound representation of Urinary bladder (black butterfly like shape) and hyperplastic prostate. An example of engineering science and medical science working together … Wikipedia
U.S. Food and Drug Administration — Infobox Government agency agency name = Food and Drug Administration parent agency = logo width = 200px logo caption = FDA Logo formed = 1906 [cite web|url=http://www.fda.gov/centennial/|title=FDA Centennial 1906 2006|accessdate=2008 09… … Wikipedia
Fentanyl — Systematic (IUPAC) name N (1 (2 phenylethyl) 4 piperidiny … Wikipedia
Galantamine — Systematic (IUPAC) name (4aS,6R,8aS) 5,6,9,10,11,12 hexahydro 3 methoxy 11 methyl 4aH [1]benzofuro[3a,3,2 ef] [2] benzazepin 6 ol Clinical data … Wikipedia
Nimodipine — Systematic (IUPAC) name 3 (2 methoxyethyl) 5 propan 2 yl 2,6 dimethyl 4 (3 nitrophenyl) 1,4 dihydropyridine 3,5 dicarboxylate Clinical data … 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
Patient safety organization — A patient safety organization (PSO) is a group, institution or association that improves medical care by reducing medical errors. In the 1990s, reports in several countries revealed a staggering number of patient injuries and deaths each year due … Wikipedia
Prescription Drug User Fee Act — The Prescription Drug User Fee Act (PDUFA) was a law passed by the United States Congress in 1992 which allowed the Food and Drug Administration (FDA) to collect fees from drug manufacturers to fund the new drug approval process. The Act provided … Wikipedia
