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How to Develop Robust Solid Oral Dosage Forms: From Conception to Post-Approval Mittal, Bhavishya (Staff Fellow, Office of Pharmaceutical Quality (OPQ), Center for Drug Evaluation and Research (CDER), US Food and Drug Administration (FDA), Silver Spring, MD, USA)
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How to Develop Robust Solid Oral Dosage Forms: From Conception to Post-Approval
Mittal, Bhavishya (Staff Fellow, Office of Pharmaceutical Quality (OPQ), Center for Drug Evaluation and Research (CDER), US Food and Drug Administration (FDA), Silver Spring, MD, USA)
How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. The book details all of the necessary steps from formulation through the post-approval phase and contains industry case studies, real world advice, and troubleshooting tips. By merging the latest scientific information with practical instructions, this book provides pharmaceutical scientists in formulation research and development with a concrete look at the key aspects in the development of solid oral dosage forms.--
190 pages
| Medios de comunicación | Libros Paperback Book (Libro con tapa blanda y lomo encolado) |
| Publicado | 13 de octubre de 2016 |
| ISBN13 | 9780128047316 |
| Editores | Elsevier Science Publishing Co Inc |
| Páginas | 190 |
| Dimensiones | 228 × 154 × 14 mm · 317 g |
