Center for Biologics Evaluation and Research (U.S.). (2007). Guidance for industry: Providing regulatory submissions to the Center for Biologics Evaluation and Research (CBER) in electronic format, lot release protocols. U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research.
Chicago Style (17th ed.) CitationCenter for Biologics Evaluation and Research (U.S.). Guidance for Industry: Providing Regulatory Submissions to the Center for Biologics Evaluation and Research (CBER) in Electronic Format, Lot Release Protocols. Rockville, MD: U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, 2007.
MLA (9th ed.) CitationCenter for Biologics Evaluation and Research (U.S.). Guidance for Industry: Providing Regulatory Submissions to the Center for Biologics Evaluation and Research (CBER) in Electronic Format, Lot Release Protocols. U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, 2007.