Description
This authoritative three-volume set is the definitive reference for pharmaceutical tablet dosage forms. Edited by renowned expert L.L. Augsburger, it covers all aspects of tablet development, formulation, and manufacturing processes.
Volume 1 addresses tablet fundamentals, raw materials, and preformulation studies. Volume 2 focuses on tablet manufacture, equipment, and process validation. Volume 3 covers quality control, testing, and regulatory compliance.
The third edition includes updated information on modern manufacturing technologies, regulatory requirements, and quality assurance standards. It serves as an essential resource for pharmaceutical scientists, formulators, quality assurance professionals, and regulatory specialists.
This hardcover edition is designed for academic institutions, pharmaceutical companies, and professional reference libraries, providing practical guidance and theoretical foundations for tablet dosage form development.
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