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010 a| 2016045904;

020 a| 9781118907337 (cloth);

020 z| 9781118907900 (Adobe PDF);

020 z| 9781118907870 (epub);

035 a| (WaSeSS)ssj0001747189;

040 a| DNLM/DLCc| DLCd| DLCd| WaSeSS;

042 a| pcc;

049 a| EREEa| NEHH;

050 00 a| RS420b| .O73 2017;

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082 00 a| 615.1/92| 23;

245 00 a| Oral formulation roadmap from early drug discovery to developmenth| [electronic resource] /c| edited by Elizabeth Kwong.;

260 a| Hoboken, NJ :b| John Wiley & Sons Inc.,c| 2017.;

300 a| x, 252 pages ;c| 25 cm;

504 a| Includes bibliographical references and index.;

505 0 a| Lead identification/optimization / Dr. Mei Wong And Dr. Mark Mcallister -- Oral drug formulation development in pharmaceutical lead selection stage / Shayne Cox Gad -- Bridging end of discovery to regulatory filing : formulations for IND- and registration-enabling nonclinical studies / Evan A. Thackaberry -- Planning the first clinical trials with clinical manufacturing organization (CMO) / Elizabeth Kwong and Caroline McGregor -- Formulation strategies for high dose toxicology studies : case studies / Dennis H. Leung, Pierre Daublain, Mengwei Hu, Kung-I Feng -- Formulation, analytical and regulatory strategies for first in human clinical trials / Lorenzo Capretto, Gerard Byrne, Sarah Trenfield, Lee Dowden, and Steven Booth.;

506 a| Available only to authorized users.;

538 a| Mode of access: World Wide Web;

650 12 a| Drug Discovery=| ^A1013013;

650 22 a| Chemistry, Pharmaceuticalx| methods=| ^A921593;

650 22 a| Clinical Trials as Topic=| ^A920927;

650 22 a| Dosage Forms=| ^A918881;

650 22 a| Administratoin, Oral?| UNAUTHORIZED;

655 0 a| Electronic books.=| ^A491897;

700 1 a| Kwong, Elizabeth,d| 1954-?| UNAUTHORIZED;

856 40 z| Full text available from Ebook Central - Academic Completeu| https://ebookcentral.proquest.com/lib/eastcarolina/detail.action?docID=4778028;

949 a| CLICK ON WEB ADDRESSw| ASISh| JOYNER188;

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596 a| 1 3 4;

998 a| 5196594;

999 a| CLICK ON WEB ADDRESSw| ASISc| 1i| 5196594-1001l| JNETm| JOYNERr| Ys| Yt| JNESSBKu| 11/1/2019x| EBOOKz| JERESOURCE;

999 a| CLICK ON WEB ADDRESSw| ASISc| 1i| 5196594-2001l| HSLELECm| HSLr| Ys| Yt| HEBKu| 11/1/2019x| EBOOKz| HERESOURCE;

999 a| CLICK ON WEB ADDRESSw| ASISc| 1i| 5196594-3001l| MNETm| JMUSICr| Ys| Yt| MNESSBKu| 11/1/2019x| EBOOKz| JERESOURCE;

Oral formulation roadmap from early drug discovery to development / edited by Elizabeth Kwong.

Other author	Kwong, Elizabeth, 1954-
Format	Electronic
Publication Info	Hoboken, NJ : John Wiley & Sons Inc., 2017.
Description	x, 252 pages ; 25 cm
Supplemental Content	Full text available from Ebook Central - Academic Complete
Subjects	Drug Discovery Chemistry, Pharmaceutical--methods. Clinical Trials as Topic Dosage Forms Administratoin, Oral

Contents	Lead identification/optimization / Dr. Mei Wong And Dr. Mark Mcallister -- Oral drug formulation development in pharmaceutical lead selection stage / Shayne Cox Gad -- Bridging end of discovery to regulatory filing : formulations for IND- and registration-enabling nonclinical studies / Evan A. Thackaberry -- Planning the first clinical trials with clinical manufacturing organization (CMO) / Elizabeth Kwong and Caroline McGregor -- Formulation strategies for high dose toxicology studies : case studies / Dennis H. Leung, Pierre Daublain, Mengwei Hu, Kung-I Feng -- Formulation, analytical and regulatory strategies for first in human clinical trials / Lorenzo Capretto, Gerard Byrne, Sarah Trenfield, Lee Dowden, and Steven Booth.
Bibliography note	Includes bibliographical references and index.
Access restriction	Available only to authorized users.
Technical details	Mode of access: World Wide Web
Genre/form	Electronic books.
LCCN	2016045904
ISBN	9781118907337 (cloth)

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Oral formulation roadmap from early drug discovery to development / edited by Elizabeth Kwong.

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