書名 | 作者 | 出版年 | 查看 | 回報錯誤連結 |
Write it down:guidance for preparing effective and compliant documentation / |
Janet Gough. |
2005 |
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GMP-Qualifizierung und Validierung von Wirkstoffanlagen:ein Leitfaden fur die Praxis / |
Ralf Gengenbach mit Beitragen von Hans-Georg Eckert und Wolfgang Hahnel. |
2008 |
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回報問題連結 |
How to validate a pharmaceutical process / |
Steven A. Ostrove. |
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回報問題連結 |
Attrition in the pharmaceutical industry:reasons, implications, and pathways forward / |
Alexander A. Alex, C. John Harris, Dennis A. Smith. |
2016 |
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回報問題連結 |
Good manufacturing practices for pharmaceuticals:a plan for total quality control from manufacturer to consumer / |
Sidney H. Willig. |
2000 |
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回報問題連結 |
Pharmaceutical process validation |
Robert A. Nash, Alfred H. Wachter. |
2003 |
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回報問題連結 |
Compliance handbook for pharmaceuticals, medical devices, and biologics |
Carmen Medina. |
2004 |
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Economic evaluation of cancer drugs:using clinical trial and real-world data / |
Iftekhar Khan, Ralph Crott, and Zahid Bashir. |
2020 |
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回報問題連結 |
Global supply chains in the pharmaceutical industry |
Hamed Nozari and Agnieszka Szmelter, editors. |
2019 |
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Social and administrative aspects of pharmacy in low- and middle-income countries :present challenges and future solutions / |
editors, Mohamed Izham Mohamed Ibrahim, Albert I. Wertheimer, Zheer-Ud-Din Babar. |
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Hygiene in der arzneimittelproduktion :Sterile und nicht-sterile Arzeneiformen / |
Michael Rieth und Norbert Krämer. |
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回報問題連結 |
Continuous manufacturing of pharmaceuticals |
Peter Kleinebudde, Johannes Khinast, Jukka Rantanen. |
2017 |
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Manufacturing of pharmaceutical proteins:from technology to economy / |
Stefan Behme. |
2022 |
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回報問題連結 |
Facility validation:theory, practice, and tools / |
Graham C. Wrigley. |
2004 |
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回報問題連結 |
Validating pharmaceutical systems:good computer practice in life science manufacturing / |
John Andrews. |
2005 |
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Industrialization of drug discovery:from target selection through lead optimization / |
Jeffrey S. Handen. |
2005 |
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