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Intelligent drug development : trials and errors in clinical research /
Clinical research is heavily regulated and involves coordination of numerous pharmaceutical-related disciplines. Each individual trial involves contractual, regulatory, and ethics approval at each site and in each country. Clinical trials have become so complex and government requirements so stringe...
| Clasificación: | Libro Electrónico |
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| Autor principal: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Oxford ; New York :
Oxford University Press,
[2014]
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| Temas: | |
| Acceso en línea: | Texto completo |
| Sumario: | Clinical research is heavily regulated and involves coordination of numerous pharmaceutical-related disciplines. Each individual trial involves contractual, regulatory, and ethics approval at each site and in each country. Clinical trials have become so complex and government requirements so stringent that researchers often approach trials too cautiously, convinced that the process is bound to be insurmountably complicated and riddled with roadblocks. A step back is needed, an objective examination of the drug development process as a whole, and recommendations made for streamlining the proces. |
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| Descripción Física: | 1 online resource (241 pages) |
| Bibliografía: | Includes bibliographical references (pages 213-215) and index. |
| ISBN: | 9780190200657 0190200650 9780199974580 0199974586 9780197563335 0197563333 |