The History of Dermatology and Dermatologists at the US Food and Drug Administration The Food and Drug Administrations Role in Dermatologic Drug Development Postmarket Assessment for Drugs and Biologics Used in Dermatology and Cutaneous Adverse Drug Reactions How Does the Food and Drug Administration Approve Topical Generic Drugs Applied to the Skin? Dermatology Drugs for Children-U.S. Food and Drug Administration Perspective Regulation of Medical Devices for Dermatology Regulation of Cosmetics in the United States Cutaneous Pharmacokinetic Approaches to Compare Bioavailability and/or Bioequivalence for Topical Drug Products Measuring What Matters to Patients in Dermatology Drug Development: A Regulatory Perspective
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