Klinični preizkusi

Ogled izdelka

Bad Pharma()

Vezava:

18,05 €

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Clinical Trials(2024) PIANTADOSI, STEVEN (BOSTON, MA, USA)

Vezava: Trda

203,14 €

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Drugs: From Discovery to Approval(2015) RICK NG

Vezava:

127,27 €

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Adverse Events - Race, Inequality, and the Testing of New Pharmaceuticals(2020) FISHER, JILL A.

Vezava: Mehka

41,79 €

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Clinical Trials: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines(2016) TOM BRODY

Vezava: Trda

125,61 €

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Design and Analysis of Cross-Over Trials(2014) JONES, BYRON,KENWARD, MICHAEL G.

Vezava: Trda

165,38 €

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Economic Evaluation of Cancer Drugs(2019) KHAN, IFTEKHAR,CROTT, RALPH,BASHIR, ZAHID (HAEMATO-ONCOLOGY, WELWYN GARDEN CITY, UK)

The first book on the design and analysis of not only clinical trials but also how observational non-interventional data using clinical data is applied to economic evaluation and re-imbursement in the context of Cancer. This book is a non technical exposi

Vezava: Trda

97,45 €

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Sample Size Calculations in Clinical Research(2020) CHOW, SHEIN-CHUNG (DUKE UNIV, USA),SHAO, JUN (DEPARTMENT OF STATISTICS, UNIVERSITY OF WISCONSIN, USA),WANG, HANSHENG,LOKHNYGINA, YULIYA (DUKE UNIVERSITY SCHOOL OF MEDICINE, DURHAM, NC, USA)

Like the well-regarded and bestselling second edition, Sample Size Calculations in Clinical Research, Third Edition, presents statistical procedures for performing sample size calculations during various phases of clinical research and development. This n

Vezava: Mehka

73,49 €

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Real-World Evidence in Drug Development and Evaluation(2022)

This book concerns use of real world data (RWD) and real world evidence (RWE) to aid drug development across product cycle. RWD are healthcare data that are collected outside the constraints of conventual controlled randomized trials (CRTs); whereas RWE i

Vezava: Mehka

78,01 €

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Estimands, Estimators and Sensitivity Analysis in Clinical Trials(2020) MALLINCKRODT, CRAIG,MOLENBERGHS, GEERT,LIPKOVICH, ILYA (QUINTILES, DURHAM, NORTH CAROLINA, USA),RATITCH, BOHDANA (ELI LILLY CANANDA, ONTARIO, CANADA)

This book will use the new guidance as a framework for developing and implementing comprehensive analysis plans for clinical trials that support the development and approval of medical interventions.

Vezava: Trda

134,37 €

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Immunity(2020) MACCIOCHI, DR JENNA

Start strengthening your immunity for good.

Vezava: Mehka

20,84 €

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Interface between Regulation and Statistics in Drug Development(2022) ALEMAYEHU, DEMISSIE,EMIR, BIROL,GAFFNEY, MICHAEL (PFIZER INC., NEW YORK)

This book provides a systematic exposition of the interplay between the two disciplines, including emerging themes pertaining to the acceleration of the development of pharmaceutical medicines to serve patients with unmet needs.

Vezava: Mehka

78,01 €