Search results
Results from the WOW.Com Content Network
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".
Pharmacy and Poisons Board of Hong Kong (PPBHK) 2016 Hungary: National Institute of Pharmacy and Nutrition (OGYÉI) 1995 Iceland: Icelandic Medicines Agency (IMA) 1995 Indonesia: National Agency for Drug and Food Control (NADFC) Badan Pengawas Obat dan Makanan Republik Indonesia (BPOM) 2012 Iran: Iran Food and Drug Administration (IFDA) 2018 ...
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.
USP establishes documentary (written) and reference (physical) standards for medicines, food ingredients, dietary supplement products, and ingredients. These standards are used by regulatory agencies and manufacturers to help to ensure that these products are of the appropriate identity, as well as strength, quality, purity, and consistency.
The organization's nearly 60,000 members include pharmacists, student pharmacists, and pharmacy technicians. [1] ASHP maintains a national database on U.S. drug shortages that is published on their website.
Martindale aims to cover drugs and related substances reported to be of clinical interest anywhere in the world. It provides health professionals with a useful source of information to identify medicines, such as confirming the drug and brand name of a medication being taken by a patient arriving from abroad.
In drug development and medical device development [1] the Investigator's Brochure (IB) is a comprehensive document summarizing the body of information about an investigational product ("IP" or "study drug") obtained during a drug trial.
Good documentation practice (recommended to abbreviate as GDocP to distinguish from "good distribution practice" also abbreviated GDP) is a term in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.