drug formulation
11Pharmaceutical formulation — Pharmaceutical formulation, in pharmaceutics, is the process in which different chemical substances, including the active drug, are combined to produce a final medicinal product. Contents 1 Stages and timeline 2 Oral formulations 2.1 Tablet form …
12New Drug Application — Regulation of therapeutic goods in the United States Prescription drugs Over the counter d …
13New drug application — The New Drug Application (NDA) is the vehicle in the United States through which drug sponsors formally propose that the FDA approve a new pharmaceutical for sale and marketing. The goals of the NDA are to provide enough information to permit FDA …
14Centre for Drug Research and Development — (CDRD) Infobox Company | company name = Centre for Drug Research and Development company type = Research and Commercialization Institute foundation = 2007 location = Vancouver, British Columbia, Canada key people = Natalie Dakers, Chief Executive …
15Thin film drug delivery — Drug film redirects here. For movies featuring substance abuse, see List of drug films. Thin film drug delivery uses a dissolving film or oral drug strip to administer drugs via absorption in the mouth (buccally or sublingually) and/or via the… …
16Food and Drug Administration — FDA redirects here. For other uses, see FDA (disambiguation). Food and Drug Administration Agency overview Formed 1906 …
17Rome Consensus for a Humanitarian Drug Policy — The Rome Consensus for a Humanitarian Drug Policy is a framework for dialogue and cooperation that commits 114 National Societies of Red Cross and Red Crescent from Africa, Asia, the Americas and Europe to promote and implement humanitarian… …
18U.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… …
19Generic drug — A generic drug (generic drugs, short: generics) is a drug defined as a drug product that is comparable to brand/reference listed drug product in dosage form, strength, route of administration, quality and performance characteristics, and intended …
20Off-licenced drug — In any country, an off licenced drug does not have a licence for human use for any indication or age group in that country. Possible uses An unlicenced drug should only be used under certain circumstances: As part of a clinical trial. When it has …
