Development and Evaluation of Drugs 2024 pdf epub mobi 電子書 下載


Development and Evaluation of Drugs

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Since its initial publication in 1993, Development and Evaluation of Drugs from Laboratory through Licensure to Market has been used as a textbook and reference for scientists in biomedical research, industry, and regulatory agencies. Updated and expanded, this second edition examines recent advances in scientific and regulatory approaches as well as changes in the way in which drugs are discovered, developed, and evaluated. The information provided outlines critical steps beginning from drug discovery in the laboratory to licensure and approval for market. Biomedical research is an intrinsically changing and evolving field. A more direct strategy for drug discovery has gradually replaced random screening of natural products. More rapid identification of key molecular structures for new drug candidates and characterization of biomolecules including proteins, polysaccharides, and nucleic acids are now possible. The ability to chemically modify cell surfaces and carbohydrate linkages has facilitated designs of the next generation of new drugs. Thoroughly discussing these issues and more, Development and Evaluation of Drugs from Laboratory through Licensure to Market, Second Edition focuses on the latest developments in the science and regulation of bringing new drugs to market, including activities of the International Commission on Harmonization.

Development and Evaluation of Drugs 2024 pdf epub mobi 電子書 下載

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發表於2024-11-17

Development and Evaluation of Drugs 2024 pdf epub mobi 電子書 下載

Development and Evaluation of Drugs 2024 pdf epub mobi 電子書 下載

Development and Evaluation of Drugs 2024 pdf epub mobi 電子書 下載



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評分

1.三個颱大畢業的華裔藥學傢的著作,相當於本科階段學習的《臨床藥學》,內容淺顯易懂,僅用於溫習迴顧。 drug development is a complicated,time-consuming,and costly process. 2.臨床前實驗: 閤理藥物設計 專利及申請 動物安全性 吸收分布代謝排泄 臨床試驗: 3...

評分

1.三個颱大畢業的華裔藥學傢的著作,相當於本科階段學習的《臨床藥學》,內容淺顯易懂,僅用於溫習迴顧。 drug development is a complicated,time-consuming,and costly process. 2.臨床前實驗: 閤理藥物設計 專利及申請 動物安全性 吸收分布代謝排泄 臨床試驗: 3...

評分

1.三個颱大畢業的華裔藥學傢的著作,相當於本科階段學習的《臨床藥學》,內容淺顯易懂,僅用於溫習迴顧。 drug development is a complicated,time-consuming,and costly process. 2.臨床前實驗: 閤理藥物設計 專利及申請 動物安全性 吸收分布代謝排泄 臨床試驗: 3...

評分

1.三個颱大畢業的華裔藥學傢的著作,相當於本科階段學習的《臨床藥學》,內容淺顯易懂,僅用於溫習迴顧。 drug development is a complicated,time-consuming,and costly process. 2.臨床前實驗: 閤理藥物設計 專利及申請 動物安全性 吸收分布代謝排泄 臨床試驗: 3...

評分

1.三個颱大畢業的華裔藥學傢的著作,相當於本科階段學習的《臨床藥學》,內容淺顯易懂,僅用於溫習迴顧。 drug development is a complicated,time-consuming,and costly process. 2.臨床前實驗: 閤理藥物設計 專利及申請 動物安全性 吸收分布代謝排泄 臨床試驗: 3...

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出版者:CRC Pr I Llc
作者:Lee, Chi-Jen/ Lee, Lucia H./ Lu, Zhengxiong
出品人:
頁數:256
譯者:
出版時間:2003-5
價格:$ 259.84
裝幀:HRD
isbn號碼:9780849314018
叢書系列:

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Development and Evaluation of Drugs 2024 pdf epub mobi 電子書 下載
想要找書就要到 本本書屋
立刻按 ctrl+D收藏本頁
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