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Pharmaceutical industry --- Drugs - Law and legislation - United States.

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Drug Evaluation --- Clinical Trials as Topic --- Pharmaceutical Preparations --- Quality Control --- Drug Approval --- Pharmacy --- Drugs --- standards --- Law and legislation --- Pharmaceutical Preparations - standards --- Pharmacy - Law and legislation - United States --- Drugs - Law and legislation - United States

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Therapeutics --- Clinical drug trials --- Drugs --- History --- Law and legislation --- Thérapeutique --- Clinical --- Experimental --- Clinical. --- Experimental. --- Thérapeutique --- Pharmacotechnology. Preparations --- Professional ethics. Deontology --- History of human medicine --- Economic law --- anno 1900-1999 --- United States --- Pharmacology --- Therapeutics. --- Médicaments --- Histoire --- Droit --- Législation --- Therapeutics - United States - History - 20th century --- Clinical drug trials - United States - History - 20th century --- Drugs - Law and legislation - United States - History - 20th century --- United States of America

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Contrary to the common belief that dietary supplements are “unregulated” in the United States, nutrients and other dietary ingredient-containing products have been regulated in this country for a little over a century at least in some capacity, initially through the Pure Food and Drug Act (PFDA) of 1906 and culminating with the many anticipated regulations to be implemented following the recent enactment of the Food Safety Modernization Act of 2010 (FSMA).   The goal of this brief is to review and discuss the current statutes and regulations surrounding the ingredients, manufacturing standards, safety, and labeling of dietary supplements for the purpose of protecting consumers.

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Advocates of rapid access to medicines and critics fearful of inadequate testing both argue that globalization will supersede national medical practices and result in the easy transfer of pharmaceuticals around the world. In Pharmacopolitics, Arthur Daemmrich challenges their assumptions by comparing drug laws, clinical trials, and systems for monitoring adverse reactions in the United States and Germany, two countries with similarly advanced systems for medical research, testing, and patient care. Daemmrich proposes that divergent ""therapeutic cultures""--the interrelationships among

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