APA (7th ed.) Citation

Center for Biologics Evaluation and Research (U.S.). (2005). Guidance for industry: MedWatch form FDA 3550A, mandatory reporting of adverse reactions related to human cells, tissues, and cellular and tissue-based products (HCT/Ps). U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research.

Chicago Style (17th ed.) Citation

Center for Biologics Evaluation and Research (U.S.). Guidance for Industry: MedWatch Form FDA 3550A, Mandatory Reporting of Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue-based Products (HCT/Ps). Rockville, MD: U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, 2005.

MLA (9th ed.) Citation

Center for Biologics Evaluation and Research (U.S.). Guidance for Industry: MedWatch Form FDA 3550A, Mandatory Reporting of Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue-based Products (HCT/Ps). U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, 2005.

Warning: These citations may not always be 100% accurate.