000 | 02125nam a22003137a 4500 | ||
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003 | OSt | ||
005 | 20241230145744.0 | ||
008 | 241230b |||||||| |||| 00| 0 hin d | ||
020 | _a9781118907276 | ||
040 |
_aNISER LIBRARY _beng _cNISER LIBRARY |
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041 | _aEnglish | ||
082 |
_a615.32 _bNG-D |
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100 | _aNg, Rick | ||
245 |
_aDrugs : _bfrom discovery to approval |
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250 | _a3rd ed. | ||
260 |
_aNew Jersey : _bWiley Blackwell, _c2015 |
||
300 | _axvi, 536p. | ||
504 | _aIncludes bibliographical references and index. | ||
520 | _aThe third edition of this best-selling book continues to offer a user-friendly, step-by-step introduction to all the key processes involved in bringing a drug to the market, including the performance of pre-clinical studies, the conduct of human clinical trials, regulatory controls, and even the manufacturing processes for pharmaceutical products. Concise and easy to read, Drugs: From Discovery to Approval, Third Edition quickly introduces basic concepts, then moves on to discuss target selection and the drug discovery process for both small and large molecular drugs. The third edition incorporates the latest developments and updates in the pharmaceutical community, provides more comprehensive coverage of topics, and includes more materials and case studies suited to college and university use. Biotechnology is a dynamic field with changes across R&D, clinical trials, manufacturing and regulatory processes, and the third edition of the text provides timely updates for those in this rapidly growing field. | ||
650 | _aDrug Discovery | ||
650 | _aChemistry, Pharmaceutical | ||
650 |
_aClinical Trials as Topic _xmethods |
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650 |
_aDrug Approval _xlegislation & jurisprudence |
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650 |
_aDrug Approval _xmethods |
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650 | _aTechnology, Pharmaceutical | ||
856 |
_3Table of Contents _uhttps://www.wiley.com/en-be/Drugs%3A+From+Discovery+to+Approval%2C+3rd+Edition-p-9781118907276#tableofcontents-section |
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856 |
_3Reviews _uhttps://www.goodreads.com/book/show/23530327-drugs?ref=nav_sb_ss_1_13#CommunityReviews |
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