Food and drug law : federal regulation of drugs, biologics, medical devices, foods, dietary supplements, personal care, veterinary and tobacco products / Roseann B. Termini, Esq.
"Contains all 12 volumes" (refers to 12 volumes available previously as separate e-books). Includes bibliographical references and index.
Contents:
The "why" of the United States Food and Drug Administration, landmark legislation, and court decisions -- Food and drug law administrative primer -- The Food and Drug Administration : criminal and civil enforcement strategies -- Medical devices and radiation emitting products regulation -- Human drug regulation : approvals, promotion, off-label, warnings, accountability, and postmarket surveillance -- Biotechnology and biologics regulation : biosimilars, allergenics, tissue, blood, vaccines and gene therapy products --The veterinary products regulation -- Personal care products regulation : cosmetic safety, terminology, product classification and enforcement -- Food regulation : safety, pathogens, recalls, claims, additives, allergens and biotechnology -- Dietary supplements, herbs and botanicals -- Tobacco products regulation -- Politics, globalization, foreign corrupt practices, product classification, professionalism and the future.
Summary:
"This food and drug law...book is organized...in order to comprehend a complex area of federal regulatory law. There is a separate volume for each subject based on regulation under the United States Federal Food, Drug and Cosmetic Act (FDCA) and related laws all contained in this bound book. [This book] is organized into subject specific titled volumes with a concise introduction to provide a particular focus for the reader."-- Provided by publisher.
This resource is supported by the Institute of Museum and Library Services under the provisions of the Library Services and Technology Act as administered by State Library of Iowa.