Expert-authored analysis, practice tools, and current awareness news combined in this source to support full compliance in all areas of healthcare regulation as well as managing reimbursement efficiently and effectively. [formerly Cheetah)
Contains annotations for all major compliance-related statues, regulations, and administrative decisions. Nexis UNI’s statutory and regulatory content is more current than the publicly available free content for the United States Code and the CFR at GovInfo.gov
The Cochrane Library includes the Cochrane Central Register of Controlled Trials (CENTRAL), a highly concentrated source of reports of randomized and quasi-randomized controlled trials. Most CENTRAL records are taken from bibliographic databases (mainly PubMed and Embase), but records are also derived from other published and unpublished sources, including CINAHL, ClinicalTrials.gov and the WHO's International Clinical Trials Registry Platform.
This resource from the National Library of Medicine provides information on drugs that have received FDA approval, including information about their usa, toxicological information, clinical trials that may be ongoing, rerferences from PubMed, and other reources.
The Food and Drug Administration Web site allows users to search for whether or not certain drugs and medical devices have been approved for general use by the public. Users can also search for current drug studies. Information is also available regarding regulations about clinical trials.