Center for Devices and Radiological Health (U.S.). (2006). Information sheet guidance for IRBs, clinical investigators, and sponsors: Significant risk and nonsignificant risk medical device studies. U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health.
Chicago Style (17th ed.) CitationCenter for Devices and Radiological Health (U.S.). Information Sheet Guidance for IRBs, Clinical Investigators, and Sponsors: Significant Risk and Nonsignificant Risk Medical Device Studies. Rockville, MD: U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, 2006.
MLA (9th ed.) CitationCenter for Devices and Radiological Health (U.S.). Information Sheet Guidance for IRBs, Clinical Investigators, and Sponsors: Significant Risk and Nonsignificant Risk Medical Device Studies. U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, 2006.