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AAPP maintains "The Mental Health Pharmacy Directory", an online search engine that includes more than 850 mental health pharmacies. [3] [4] As of December 2015, AAPP is a member of the Coalition on Psychiatric Emergencies (COPE) and is the only professional pharmacy organization represented on the coalition.
The National Council for Prescription Drug Programs (NCPDP) is an American nonprofit standards development organization representing most sectors of the U.S. pharmacy services industry. It was founded in 1977 as the extension of a Drug Ad Hoc Committee that made recommendations for the U.S. National Drug Code (NDC).
The following is a partial list of the "N" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).. This list continues the information at List of MeSH codes (N03).
libtorrent is an open-source implementation of the BitTorrent protocol. It is written in and has its main library interface in C++.Its most notable features are support for Mainline DHT, IPv6, HTTP seeds and μTorrent's peer exchange. libtorrent uses Boost, specifically Boost.Asio to gain its platform independence.
b. Developing guidelines (standards) for appropriate drug use c. Assess the effectiveness of medication d. Enhance accountability in drug use e. Control medical expenses f. Prevention of drug-related problems such as adverse drug reactions, treatment failure, overuse, under-use, incorrect dosage and use of over-the-counter drugs g.
Pharmacy information systems are a potential source of valuable information for pharmaceutical companies as it contains information about the prescriber's prescribing habits. Prescription data mining of such data is a developing, specialized field. [55] Many prescribers lack the digitized information systems that reduce prescribing errors. [56]
USP 800 (Hazardous Drugs—Handling in Healthcare Settings) is a guideline created by the United States Pharmacopeia Convention (USP), as one of their General Chapters through which the USP "sets quality standards for medicines, dietary supplements and food ingredients".
A trial master file contains essential documents for a clinical trial that may be subject to regulatory agency oversight. In the European Union (EU), TMFs have a different definition and set of requirements than in the US.