Administrative procedures for CLIA categorization: guidance for industry and Food and Drug Administration staff Administrative procedures for CLIA categorization: guidance for industry and Food and Drug Administration staff

Collection: Health Policy and Services Research Series Title(s): Guidance for industry Contributor(s): United States. Department of Health and Human Services, issuing body. United States. Food and Drug Administration, issuing body. Center for Devices and Radiological Health (U.S.). Office of In Vitro Diagnostics and Radiological Health, issuing body. Publication: Silver Spring, MD : Center for Devices and Radiological Health, October 2, 2017 Language(s): English Format: Text Subject(s): Clinical Laboratory Techniques Device Approval -- standards United States United States. Department of Health and Human Services United States. Food and Drug Administration Genre(s): Guideline Technical Report Copyright: The National Library of Medicine believes this item to be in the public domain. (More information) Extent: 1 online resource (1 PDF file (10 pages)). NLM Unique ID: 101719834 (See catalog record) Permanent Link: http://resource.nlm.nih.gov/101719834