Background
Lawrence, C. Stephen was born on January 13, 1948 in Long Branch, New Jersey, United States.
Lawrence, C. Stephen was born on January 13, 1948 in Long Branch, New Jersey, United States.
University of Maine (Bachelor of Arts, 1972). Catholic University School of Law (Juris Doctor, 1984).
Worked at Hogan & Hartson L.L.P. (Washington, DC) specializing in Drug and Medical Device Regulation, Food and Drug Regulation, Food, Drug and Cosmetic Law. Admitted to the bar, 1984, Virginia. 1986, District of Columbia.
1993, California.
Member, Catholic University of America Law Review, 1983-1984. Author: "George Washington University V. Weintraub: Implied Warranty of Habitability as a (Ceremonial?) Sword," 33 Catholic University Law Review 1137, 1984. "In re Goldberg: Standards for Imposing Concurrent Reciprocal Bar Discipline," 33 Catholic University Law Review 1165, 1984.
"FDA Inspection of Clinical Research Sponsors and Investigators: Avoiding the Pitfalls," 22 Drug Information Journal 207, 1988. Co-Author: "FDA Will Regulate Bovine Interferon as an Animal Drug," 3 Genetic Engineering News 1, 1983. "A New Era for Clinical Studies of Medical Devices," Medical Device and Diagnostics Industries, May 1994;"GMP's and ISO 9000: Beware the Differences," Regulatory Affairs Focus, March 1996, AT 8.
Investigator and Consumer Safety Officer, Food and Drug Administration, 1972-1983. Member: District of Columbia Bar. Virginia, Federal (Co-Chairperson, Food and Drug Committee, 1986-1989.
Chairperson, Food and Drug Committee, 1995) and American (Member, Sections on: Administrative Law. Science and Technology) Bar Associations. Virginia State Bar; State Bar of California.
(Also practicing individually, Newport Beach, California).
Author: "George Washington University V. Weintraub: Implied Warranty of Habitability as a (Ceremonial?) Sword," 33 Catholic University Law Review 1137, 1984. "In re Goldberg: Standards for Imposing Concurrent Reciprocal Bar Discipline," 33 Catholic University Law Review 1165, 1984. "FDA Inspection of Clinical Research Sponsors and Investigators: Avoiding the Pitfalls," 22 Drug Information Journal 207, 1988.
Co-Author: "FDA Will Regulate Bovine Interferon as an Animal Drug," 3 Genetic Engineering News 1, 1983. "A New Era for Clinical Studies of Medical Devices," Medical Device and Diagnostics Industries, May 1994
"GMP's and ISO 9000: Beware the Differences," Regulatory Affairs Focus, March 1996, AT 8. Investigator and Consumer Safety Officer, Food and Drug Administration, 1972-1983.
Member, Catholic University of America Law Review, 1983-1984.