Background
Kingham, Richard F. was born on August 2, 1946 in Lafayette, Indiana, United States.
- Photos
- Works
- Photos
- Works
Other Work
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Author: "New European Medicines Agency," Food and Drug L.J., 1994 (with P. Bogaert and P. Eddy). "A Comparison of the United States. and European Approaches to Medicines Regulation," European Pharma L. Rept., 1994. "New European Medicines Agency," Japan Pharmaceuticals Monthly, 1993 (with M. Kitamura).
"Regulation of Medical Devices in the European Community," Food and Drug L.J., 1992. "Update on European Product Liability Legislation," World Pharmaceutical Standards Review, 1991 (with P. Eddy). "Medical Device Law Highlights Productive Session in Congress," World Pharmaceutical Standards Review, 1990.
"FDA Action on Sunscreens Highlights Effects of Rules on Foreign Trade," World Pharmaceutical Standards Review, 1990. "The Adverse Effects of Standardless Punitive Damage Awards on Pharmaceutical Development and Availability," Food and Drug Cosm. L.J., 1990 (with B.N. Kuhlik).
"History of FDA Regulation of Clinical Research," Drug Information J., 1988. "Das US-amerikanische Zulassungsverfahren f�r Arzneimittel: Verfahren f�r Zweitanmeldungen und Vorschlg�ge zur Verl�ngerung der Patentlaufzeit," Pharma - Recht, 1985. "Proposed Revisions of FDA's New Drug Regulations," Food Drug Cosm.
L.J., 1983 -
"The Effects of United States. Regulatory Requirements on International Pharmaceutical Marketing and Research," Proceedings of the 73rd Annual Meeting of the American Society of International Law, 1979. "Proposed Drug Regulation Reform Act of 1978," Food Drug Cosm.
L.J., 1978.
Richard F. Kingham
Edit ProfileEducation
George Washington University (Bachelor of Arts, 1968). University of Virginia (Juris Doctor, 1973).
Career
Worked at Covington & Burling. Admitted to the bar, 1973, District of Columbia. Registered foreign lawyer, England and Wales.
Order of the Coif. Articles Editor, Virginia Law Review, 1972-1973. Lecturer, University of Virginia School of Law, 1977-1990. Author: "New European Medicines Agency," Food and Drug L.J., 1994 (with P. Bogaert and P. Eddy).
"A Comparison of the United States. and European Approaches to Medicines Regulation," European Pharma L. Rept., 1994. "New European Medicines Agency," Japan Pharmaceuticals Monthly, 1993 (with M. Kitamura). "Regulation of Medical Devices in the European Community," Food and Drug L.J., 1992.
"Update on European Product Liability Legislation," World Pharmaceutical Standards Review, 1991 (with P. Eddy). "Medical Device Law Highlights Productive Session in Congress," World Pharmaceutical Standards Review, 1990. "FDA Action on Sunscreens Highlights Effects of Rules on Foreign Trade," World Pharmaceutical Standards Review, 1990.
"The Adverse Effects of Standardless Punitive Damage Awards on Pharmaceutical Development and Availability," Food and Drug Cosm. L.J., 1990 (with B.N. Kuhlik). "History of FDA Regulation of Clinical Research," Drug Information J., 1988.
"Das US-amerikanische Zulassungsverfahren für Arzneimittel: Verfahren für Zweitanmeldungen und Vorschlgäge zur Verlängerung der Patentlaufzeit," Pharma - Recht, 1985. "Proposed Revisions of FDA's New Drug Regulations," Food Drug Cosm. L.J., 1983; "The Effects of United States.
Regulatory Requirements on International Pharmaceutical Marketing and Research," Proceedings of the 73rd Annual Meeting of the American Society of International Law, 1979. "Proposed Drug Regulation Reform Act of 1978," Food Drug Cosm. L.J., 1978. Member, Committee on Issues and Priorities for New Vaccine Development, Institute of Medicine, National Academy of Sciences, 1983-1986.
National Advisory Allergy and Infectious Diseases Council, National Institutes of Health, 1988-1992. Advisory Board, World Pharmaceuticals Report, 1990. Food Law Group (United Kingdom).
Drug Information Association. Brussels Pharma Law Group. European Society of Pharmacovigilance.
(Resident, London, England Office).
Works
Other Work
-
Author: "New European Medicines Agency," Food and Drug L.J., 1994 (with P. Bogaert and P. Eddy). "A Comparison of the United States. and European Approaches to Medicines Regulation," European Pharma L. Rept., 1994. "New European Medicines Agency," Japan Pharmaceuticals Monthly, 1993 (with M. Kitamura).
"Regulation of Medical Devices in the European Community," Food and Drug L.J., 1992. "Update on European Product Liability Legislation," World Pharmaceutical Standards Review, 1991 (with P. Eddy). "Medical Device Law Highlights Productive Session in Congress," World Pharmaceutical Standards Review, 1990.
"FDA Action on Sunscreens Highlights Effects of Rules on Foreign Trade," World Pharmaceutical Standards Review, 1990. "The Adverse Effects of Standardless Punitive Damage Awards on Pharmaceutical Development and Availability," Food and Drug Cosm. L.J., 1990 (with B.N. Kuhlik).
"History of FDA Regulation of Clinical Research," Drug Information J., 1988. "Das US-amerikanische Zulassungsverfahren f�r Arzneimittel: Verfahren f�r Zweitanmeldungen und Vorschlg�ge zur Verl�ngerung der Patentlaufzeit," Pharma - Recht, 1985. "Proposed Revisions of FDA's New Drug Regulations," Food Drug Cosm.
L.J., 1983 -
"The Effects of United States. Regulatory Requirements on International Pharmaceutical Marketing and Research," Proceedings of the 73rd Annual Meeting of the American Society of International Law, 1979. "Proposed Drug Regulation Reform Act of 1978," Food Drug Cosm.
L.J., 1978.
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Membership
Member, Committee on Issues and Priorities for New Vaccine Development, Institute of Medicine, National Academy of Sciences, 1983-1986. National Advisory Allergy and Infectious Diseases Council, National Institutes of Health, 1988-1992. Advisory Board, World Pharmaceuticals Report, 1990.
Food Law Group (United Kingdom). Drug Information Association. Brussels Pharma Law Group.
European Society of Pharmacovigilance. (Resident, London, England Office).
