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U.S. Biological Warfare and Biological Defense Programs (From Medical Aspects of Chemical and Biological Warfare, P 425-436, 1997, Frederick R. Sidell, M.D., Ernest T. Takafuji, M.D., eds, et al., -- See NCJ-190599)

NCJ Number
190614
Author(s)
David R. Franz D.V.M; Cheryl D. Parrott; Ernest T. Takafuji M.D.
Date Published
1997
Length
12 pages
Annotation

This document focuses on the United States Biological Warfare Program and biological defense programs.

Abstract

In 1941, biological warfare was declared feasible and steps were taken to reduce United States vulnerability and conduct research to explore the potential of bacteriological weapons. The idea of biological weaponry was controversial, since little was known about the predictability or effectiveness of biological weapons in wartime. It was concern about the Japanese biological warfare threat that motivated the U.S. to begin to develop biological weapons. During the next 28 years, the U.S. initiative evolved into an effective, military-driven research and acquisition program, shrouded in controversy and secrecy. Most research and development was done at Fort Detrick, Maryland, while production and testing occurred at Pine Bluff, Arkansas, and Dugway Proving Ground, Utah. Field-testing was done secretly and successfully with simulants and actual agents disseminated over wide areas. A small defensive effort paralleled the weapons development and production program. With the presidential decision in 1969 to halt offensive biological weapons production, and the agreement in 1972 at the international Biological Weapons Convention never to develop, produce, stockpile, or retain biological agents or toxins, the program became entirely defensive, with medical and nonmedical components. The U.S. Biological Defense Research Program exists today, conducting research to develop physical and medical countermeasures to protect service members and civilians from the threat of modern biological warfare. 19 references