1. Dr. Daniel Acosta and In Vitro toxicology at the U.S. Food and Drug Administration's National Center for Toxicological Research
- Author
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Yiying Wang, Elvis Cuevas, Qiang Shi, Syed Sarim Imam, Dayton M. Petibone, William Slikker, Hector Rosas-Hernandez, Xuefei Cao, Rui Xiong, Syed F. Ali, Amy L. Inselman, Beverly Lyn-Cook, William B. Mattes, Li Pang, Matthew White, Cheng Wang, Priya Tripathi, Susan M. Lantz, Jennifer M. Shemansky, Robert H. Heflich, and Fang Liu
- Subjects
0301 basic medicine ,medicine.medical_specialty ,Biomedical Research ,business.industry ,United States Food and Drug Administration ,Human Development ,In vitro toxicology ,General Medicine ,History, 20th Century ,Toxicology ,History, 21st Century ,Models, Biological ,United States ,Food and drug administration ,03 medical and health sciences ,030104 developmental biology ,0302 clinical medicine ,030220 oncology & carcinogenesis ,Family medicine ,Toxicity Tests ,medicine ,Animals ,Humans ,business - Abstract
For the past five years, Dr. Daniel Acosta has served as the Deputy Director of Research at the National Center for Toxicological Research (NCTR), a principle research laboratory of the U.S. Food and Drug Administration (FDA). Over his career at NCTR, Dr. Acosta has had a major impact on developing and promoting the use of in vitro assays in regulatory toxicity and product safety assessments. As Dr. Acosta nears his retirement we have dedicated this paper to his many accomplishments at the NCTR. Described within this paper are some of the in vitro studies that have been conducted under Dr. Acosta's leadership. These studies include toxicological assessments involving developmental effects, and the development and application of in vitro reproductive, heart, liver, neurological and airway cell and tissue models.
- Published
- 2018