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010 a| 2015957914;

020 a| 9780128042175 (hardback);

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100 1 a| Brody, Tom.;

245 10 a| Clinical trialsh| [electronic resource] :b| study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines /c| Tom Brody, PH.D.;

250 a| Second edition.;

260 a| Amsterdam ;a| Boston :b| Elsevier/AP,c| 2016.;

300 a| xxxii, 863 pages :b| illustrations ;c| 24 cm;

506 a| Available only to authorized users.;

538 a| Mode of access: World Wide Web;

650 0 a| Clinical trials.;

650 0 a| Drug approval.;

655 0 a| Electronic books.;

856 40 z| Full text available from eBook - Pharmacology, Toxicology and Pharmaceutical Science 2016 [EBCPTPS16]u| https://go.openathens.net/redirector/ecu.edu?url=https%3A%2F%2Fwww.sciencedirect.com%2Fscience%2Fbook%2F9780128042175;

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999 a| CLICK ON WEB ADDRESSw| ASISc| 1i| 4696729-3001l| MNETm| JMUSICr| Ys| Yt| MNESSBKu| 5/19/2017x| EBOOKz| JERESOURCE;

Clinical trials study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines / Tom Brody, PH.D.

Author/creator	Brody, Tom
Format	Electronic
Edition	Second edition.
Publication Info	Amsterdam ; Boston : Elsevier/AP, 2016.
Description	xxxii, 863 pages : illustrations ; 24 cm
Supplemental Content	Full text available from eBook - Pharmacology, Toxicology and Pharmaceutical Science 2016 [EBCPTPS16]
Subjects	Clinical trials. Drug approval.

Access restriction	Available only to authorized users.
Technical details	Mode of access: World Wide Web
Genre/form	Electronic books.
LCCN	2015957914
ISBN	9780128042175 (hardback)

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Library	Location	Call Number	Status	Item Actions
	Electronic Resources	Access Content Online	✔ Available

Clinical trials study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines / Tom Brody, PH.D.

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