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...
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| Format: | eBook |
| Language: | English |
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New York, NY :
Oxford University Press,
2020.
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| Subjects: | |
| Online Access: | Connect to the full text of this electronic book |
| Summary: | 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, anobjective examination of the drug development process as a whole, and recommendations made for streamlining the process at all stages. With this book, Tansey systematically addresses the key elements that affect the quality, timeliness, and cost-effectiveness of the drug-development process, and identifies steps that can be adjusted and made more efficient. |
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| Item Description: | Previously issued in print: 2014. |
| Physical Description: | 1 online resource (240 pages) : illustrations |
| Audience: | Specialized. |
| Bibliography: | Includes bibliographical references and index. |
| ISBN: | 9780197563335 0197563333 |