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Drug Research and Development

JAMA. 1949;139(16):1121. doi:10.1001/jama.1949.02900330073034.
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ABSTRACT

Each of the authors provides at least one chapter dealing with that phase of the general topic which, through actual experience, he is eminently prepared to present. The thorough scope of the work can best be presented through the chapter headings which follow:

The Modern Drug Formula Drug Trade-marks and Labels Chemistry of the Formula Drug Regulation Pharmacology of the Formula New Drug Applications Laboratory Research Biologic Control Regulations Development of Biologicals Drug Certification Clinical Testing Council Acceptance Development of Facilities and Product Development, Promotion Controls and Marketing Labels and Labeling Advertising Packaging and Storage "Detailing" the Physician The Product and the Patent Professional Acceptance Law Retail Price Maintenance

As the chapter heads indicate, every possible phase of the subject has been covered, making the book the first of its

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The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. The AMA designates this journal-based CME activity for a maximum of 1 AMA PRA Category 1 CreditTM per course. Physicians should claim only the credit commensurate with the extent of their participation in the activity. Physicians who complete the CME course and score at least 80% correct on the quiz are eligible for AMA PRA Category 1 CreditTM.
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