a new drug
11Compassionate Investigational New Drug program — The Compassionate Investigational New Drug program, or Compassionate IND, is a United States Federal Government ran Investigational New Drug program that allows a limited number of patients to use medical marijuana grown at the University of… …
12I Want a New Drug — Infobox Single Name = I Want a New Drug Artist = Huey Lewis The News from Album = Sports B side = Finally Found a Home Released = 1984 Format …
13investigative new drug — Pharm. a regulatory classification assigned by the U.S. Food and Drug Administration to an unproven drug, allowing its use in approved studies with human patients. Abbr.: IND * * * …
14investigative new drug — Pharm. a regulatory classification assigned by the U.S. Food and Drug Administration to an unproven drug, allowing its use in approved studies with human patients. Abbr.: IND …
15Drug development — Drug research redirects here. For the journal, see Drug Research (journal). Drug development is a blanket term used to define the process of bringing a new drug to the market once a lead compound has been identified through the process of drug… …
16Drug Price Competition and Patent Term Restoration Act — Acronym Hatch Waxman amendments Citations Codification …
17Drug liberalization — is the process of eliminating or reducing drug prohibition laws. Variations of drug liberalization (also spelled liberalisation) include drug relegalization, drug legalization, and drug decriminalization [1] Contents 1 Policies 1.1 Drug re… …
18Drug Master File — or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory authority in the intended drug market. There is no regulatory requirement to file a DMF. However, the document… …
19Drug allergy — Classification and external resources ICD 10 T88.7 ICD 9 995.27 A drug allergy is an allergy to a drug, most commonly a medication. Medical attention …
20Drug Efficacy Study Implementation — (DESI) was a program begun by the Food and Drug Administration (FDA) in the 1960s after the requirement (in the Kefauver Harris Drug Control Act) that all drugs be efficacious as well as safe. The DESI program was intended to classify all pre… …
