Searchable U.S. Federal Regulations for GCP, GLP, HIPAA and drug registration
Good research Practices provides the U.S. federal regulations that govern the standards for conducting applied research into drugs, biologics and devices for human health, as well as the regulations for the application of that research to gain approval for commercialization of drugs, biologics and devices in the U.S. Content is from a U.S. government website (https://www.ecfr.gov) of open data that provides the Code of Federal Regulations. Included are 21 CFR Parts 11, 50, 54, 56, 58, 99, 312, 316, 320, 361, 601, 807, 812, 814 and 45 CFR Parts 160, 162, 164. Good research Practices is developed and distributed by Elchland Software (a private, independent entity with no government affiliation).