Background
Kahan, Jonathan S. was born on April 5, 1948 in New York, New York, United States.
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- Works
- Photos
- Works
Other Work
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Author: "Medical Devices: Obtaining FDA Market Clearance," (Parexel 1995). "The New Enforcement Provisions of the Safe Medical Devices Act of 1990," 46 Food Drug Cosmetic Law Journal 177 (1991). "Legal Implications of Software Validation in Pharmaceutical Manufacturing," 21 Drug Information Journal 481, 1987.
"Regulation of Computer Hardware and Software as Medical Devices," 4 Canadian Computer Law Reporter 50, 1987. "Medical Device Reclassification: The Evolution of FDA Policy," 42 Food Drug Cosmetic Law Journal 288, 1987. "The Evolution of FDA Regulation of New Medical Device Technology and Product Applications," 41 Food, Drug, Cosmetic Law Journal 207, 1986.
"Premarket Approval Versus Premarket Notification: Different Routes to the Same Market," 39 Food, Drug, Cosmetic Law Journal, 1984. "The Effect of Proposed Food Safety Legislation on Colors," 39 Food Drug, Cosmetic Law Journal, 1984. "Reporting of Substantial Product Hazards Under Section 15 of the Consumer Product Safety Act," 30 Administrative Law Review 289, 1978.
"Reporting Substantial Risks Under Section 8(e) of the Toxic Substances Control Act," 19 Boston College Law Review 859, 1978. "Criminal Liability Under the Federal Food, Drug and Cosmetic Act - the Large Corporation Perspective," 36 Food, Drug, Cosmetic Law Journal 314, 1981. "Laser and Electronic Medical Devices - An Overview of Food and Drug Administration Regulation," 38 Food, Drug, Cosmetic Law Journal 220, 1983.
Co-Author: "Expedited Availability of New Drugs," 45 Food Drug Cosmetic Law Journal 81, 1990. "Federal Regulation of Food and Food Additive Biotechnology," 38 Administrative Law Review 1, 1986. "The Impact on Medical Malpractice Cases of Food and Drug Administration Regulation," 20 The Forum 418, 1985.
"Recent Developments Regarding Look-Alike Drugs," 35 Food, Drug, Cosmetic Law Journal 4, 1980.
Jonathan S. Kahan
Edit ProfileEducation
George Washington University (Bachelor of Arts, 1970. Juris Doctor, 1973).
Career
Worked at Hogan & Hartson L.L.P. (Washington, DC) specializing in Food and Drug Regulation, Food, Drug and Cosmetic Law, Drug and Medical Device Regulation. Admitted to the bar, 1973, District of Columbia. Phi Beta Kappa; Phi Eta Sigma.
Order of the Coif. Member, George Washington Law Review, 1971-1973. Contributing Editor: Medical Device and Diagnostic Industry Magazine, 1984. Clinica Magazine, 1987.
Member, Editorial Advisory Board, Food Drug Cosmetic Law Journal, 1988-1992. Law Clerk to Judge Oliver Gasch, United States. District Court for the District of Columbia, 1973-1974.
Author: "Medical Devices: Obtaining FDA Market Clearance," (Parexel 1995). "The New Enforcement Provisions of the Safe Medical Devices Act of 1990," 46 Food Drug Cosmetic Law Journal 177 (1991). "Legal Implications of Software Validation in Pharmaceutical Manufacturing," 21 Drug Information Journal 481, 1987.
"Regulation of Computer Hardware and Software as Medical Devices," 4 Canadian Computer Law Reporter 50, 1987. "Medical Device Reclassification: The Evolution of FDA Policy," 42 Food Drug Cosmetic Law Journal 288, 1987. "The Evolution of FDA Regulation of New Medical Device Technology and Product Applications," 41 Food, Drug, Cosmetic Law Journal 207, 1986.
"Premarket Approval Versus Premarket Notification: Different Routes to the Same Market," 39 Food, Drug, Cosmetic Law Journal, 1984. "The Effect of Proposed Food Safety Legislation on Colors," 39 Food Drug, Cosmetic Law Journal, 1984. "Reporting of Substantial Product Hazards Under Section 15 of the Consumer Product Safety Act," 30 Administrative Law Review 289, 1978.
"Reporting Substantial Risks Under Section 8(e) of the Toxic Substances Control Act," 19 Boston College Law Review 859, 1978. "Criminal Liability Under the Federal Food, Drug and Cosmetic Act - the Large Corporation Perspective," 36 Food, Drug, Cosmetic Law Journal 314, 1981. "Laser and Electronic Medical Devices - An Overview of Food and Drug Administration Regulation," 38 Food, Drug, Cosmetic Law Journal 220, 1983.
Co-Author: "Expedited Availability of New Drugs," 45 Food Drug Cosmetic Law Journal 81, 1990. "Federal Regulation of Food and Food Additive Biotechnology," 38 Administrative Law Review 1, 1986. "The Impact on Medical Malpractice Cases of Food and Drug Administration Regulation," 20 The Forum 418, 1985.
"Recent Developments Regarding Look-Alike Drugs," 35 Food, Drug, Cosmetic Law Journal 4, 1980. Member: The District of Columbia Bar. Bar Association of the District of Columbia (Co-Chairman, Steering Committee, Section on Administrative Law and Agency Practice, 1987-1992).
Federal (Chairman, Health and Human Services Section, 1983-1989) and American (Member, Sections on: Antitrust Law. Administrative Law; Business Law. Member, Food, Drug and Cosmetic Law Committee, 1982-1992) Bar Associations.
Works
book
Other Work
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Author: "Medical Devices: Obtaining FDA Market Clearance," (Parexel 1995). "The New Enforcement Provisions of the Safe Medical Devices Act of 1990," 46 Food Drug Cosmetic Law Journal 177 (1991). "Legal Implications of Software Validation in Pharmaceutical Manufacturing," 21 Drug Information Journal 481, 1987.
"Regulation of Computer Hardware and Software as Medical Devices," 4 Canadian Computer Law Reporter 50, 1987. "Medical Device Reclassification: The Evolution of FDA Policy," 42 Food Drug Cosmetic Law Journal 288, 1987. "The Evolution of FDA Regulation of New Medical Device Technology and Product Applications," 41 Food, Drug, Cosmetic Law Journal 207, 1986.
"Premarket Approval Versus Premarket Notification: Different Routes to the Same Market," 39 Food, Drug, Cosmetic Law Journal, 1984. "The Effect of Proposed Food Safety Legislation on Colors," 39 Food Drug, Cosmetic Law Journal, 1984. "Reporting of Substantial Product Hazards Under Section 15 of the Consumer Product Safety Act," 30 Administrative Law Review 289, 1978.
"Reporting Substantial Risks Under Section 8(e) of the Toxic Substances Control Act," 19 Boston College Law Review 859, 1978. "Criminal Liability Under the Federal Food, Drug and Cosmetic Act - the Large Corporation Perspective," 36 Food, Drug, Cosmetic Law Journal 314, 1981. "Laser and Electronic Medical Devices - An Overview of Food and Drug Administration Regulation," 38 Food, Drug, Cosmetic Law Journal 220, 1983.
Co-Author: "Expedited Availability of New Drugs," 45 Food Drug Cosmetic Law Journal 81, 1990. "Federal Regulation of Food and Food Additive Biotechnology," 38 Administrative Law Review 1, 1986. "The Impact on Medical Malpractice Cases of Food and Drug Administration Regulation," 20 The Forum 418, 1985.
"Recent Developments Regarding Look-Alike Drugs," 35 Food, Drug, Cosmetic Law Journal 4, 1980.
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Membership
Member, George Washington Law Review, 1971-1973.
