drug inspection
41Good manufacturing practice — or GMP are practices and the systems required to be adapted in pharmaceutical manufacturing, quality control, quality system covering the manufacture and testing of pharmaceuticals or drugs including active pharmaceutical ingredients, diagnostics …
42Gun laws in the United States (by state) — U.S. Firearms Legal Topics Assault weapons ban ATF Bureau Brady Handgun Violence Prevention Act Concealed carry in the U.S. Domestic Violence Offender Gun Ban …
43List of Statutory Instruments of the United Kingdom, 1993 — This is a complete list of all 1844 Statutory Instruments published in the United Kingdom in the year 1993. NOTOC 1 100* Environmental Protection (Controls on Injurious Substances) Regulations 1993 S.I. 1993/1 * Rail Crossing Extinguishment and… …
44Office of Criminal Investigations — FDA OCI logo The Office of Criminal Investigations (OCI) was established to provide the Food and Drug Administration (FDA) with a specific Office to conduct and coordinate criminal investigations. OCI special agents employ customary federal law… …
45Hazard Analysis and Critical Control Points — (HACCP) is a systematic preventive approach to food safety and pharmaceutical safety that addresses physical, chemical, and biological hazards as a means of prevention rather than finished product inspection. HACCP is used in the food industry to …
46Mexico–United States border — The border between the United States and Mexico spans four U.S. states, six Mexican states, and has over twenty commercial railroad crossings …
47diagnosis — /duy euhg noh sis/, n., pl. diagnoses / seez/. 1. Med. a. the process of determining by examination the nature and circumstances of a diseased condition. b. the decision reached from such an examination. Abbr.: Dx 2. Biol. scientific… …
48Genetically modified organism — GMO redirects here. For other uses, see GMO (disambiguation). GloFish, the first genetically modified animal to be sold as a pet A genetically modified organism (GMO) or genetically engineered organism (GEO) is an organism whose genetic material… …
49Office of Regulatory Affairs — The Office of Regulatory Affairs (ORA)[1] is the part of the U.S. Food and Drug Administration (FDA) that enforces the laws governing biologics, cosmetics, drugs, food, medical devices, radiation emitting electronic devices, tobacco products, and …
50Health and Disease — ▪ 2009 Introduction Food and Drug Safety. In 2008 the contamination of infant formula and related dairy products with melamine in China led to widespread health problems in children, including urinary problems and possible renal tube… …
