Generic Drug Product Development: Solid Oral Dosage Forms
"This book collects in-depth discussions from more than 30 noted specialists on topics such as quality control, experimental formulations, pharmaceutical ingredients, conventional and modified-release products, and bioequivalence. It considers key elements in the formulation of generic drug pro...
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| Другие авторы: | , |
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| Формат: | |
| Язык: | английский |
| Опубликовано: |
New York
CRC Press is an Imprint of Taylor & Francis Group
2020
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| Редактирование: | 2nd ed. |
| Серии: | Drugs and The Pharmaceutical Sciences Series
Vol - 212 |
| Предметы: | |
| Метки: |
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| Итог: | "This book collects in-depth discussions from more than 30 noted specialists on topics such as quality control, experimental formulations, pharmaceutical ingredients, conventional and modified-release products, and bioequivalence. It considers key elements in the formulation of generic drug products including the availability of raw materials and chemical purity. It contains new chapters on experimental formulation development, and the relationship between the FDA and the United States Pharmacopeia" |
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| Объем: | xii, 385 p. |
| ISBN: | 9780367894894 |