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Analysis of Drug Impurities - Sheffield Analytical Chemistry Series Smith
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Analysis of Drug Impurities - Sheffield Analytical Chemistry Series
Smith
A key component of the overall quality of a pharmaceutical is control of impurities, as their presence, even in small amounts, may affect drug safety and efficacy. The identification and quantification of impurities to acceptable standards presents a significant challenge to the analytical chemist.
288 pages, Illustrations
| Mediji | Grāmatas Hardcover Book (Grāmata ar cieto muguriņu un vāku) |
| Izlaists | 2007. gada 4. aprīlis |
| ISBN13 | 9781405133586 |
| Izdevēji | John Wiley and Sons Ltd |
| Lapas | 288 |
| Izmēri | 242 × 161 × 22 mm · 664 g |
| Redaktors | Smith, Richard J. (GlaxoSmithKline, Stevenage, Herfordshire, UK) |
| Redaktors | Webb, Michael L. (GlaxoSmithKline, Stevenage, Herfordshire, UK) |