Scaleup of immediate release oral solid dosage forms.
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Chemistry, Pharmaceutical↗
Biomedical subjects
Publications and source records attributed to H M Arbit.
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Federal regulations governing the introduction of new drugs in the United States are reviewed. The discussion includes the legislative background, what constitutes a "new drug," drug development, investigational new drugs, new drug applications, pharmacist involvement in clinical trials, the approval process and postmarketing surveillance.
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Explore the source record for details and available documents.