| 000 | 01059nam a22003017a 4500 | ||
|---|---|---|---|
| 003 | OSt | ||
| 005 | 20250128145044.0 | ||
| 008 | 250128b |||||||| |||| 00| 0 eng d | ||
| 020 | _a9780128042175 (hardcover) | ||
| 040 |
_aNUST _beng _cNUST _dNUST _erda |
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| 050 | _aR853 BRO | ||
| 100 |
_aBrody, Tom _eAuthor |
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| 245 |
_aClinical trials : _bstudy design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines / _cTom Brody |
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| 250 | _aSecond edition | ||
| 260 |
_aAmsterdam : _bElsevier/Academic Press, _c2016. |
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| 300 |
_axxxii, 863 pages : _billustrations ; _c24 cm. |
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| 336 |
_2rdamedia _atext _btxt |
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| 337 |
_2rdamedia _aunmediated _bn |
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| 338 |
_2rdamedia _avolume _bnc |
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| 504 | _aIncludes bibliographical references and index. | ||
| 650 | _vClinical trials -- Design. | ||
| 650 | _vDrugs -- Testing. | ||
| 650 | _vClinical Trials as Topic | ||
| 650 | _vDrug Approval. | ||
| 650 | _vResearch Design. | ||
| 650 | _vClinical Trials Data Monitoring Committees. | ||
| 942 |
_2lcc _cBOOKS _hR853 BRO _kR _mBRO _n0 |
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| 999 |
_c171208 _d171208 |
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