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Fundamental Concepts for New Clinical Trialists (Record no. 1160)

MARC details
000 -LEADER
fixed length control field 02356 a2200337 4500
001 - CONTROL NUMBER
control field 0367783398
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250317100400.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 250312042021xx eng
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9780367783396
037 ## - SOURCE OF ACQUISITION
Source of stock number/acquisition Taylor & Francis
Terms of availability GBP 47.99
Form of issue BB
040 ## - CATALOGING SOURCE
Original cataloging agency 01
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title eng
072 7# - SUBJECT CATEGORY CODE
Subject category code PS
Source thema
072 7# - SUBJECT CATEGORY CODE
Subject category code TDCW
Source thema
072 7# - SUBJECT CATEGORY CODE
Subject category code MBGR1
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072 7# - SUBJECT CATEGORY CODE
Subject category code PBT
Source thema
072 7# - SUBJECT CATEGORY CODE
Subject category code PS
Source bic
072 7# - SUBJECT CATEGORY CODE
Subject category code TDCW
Source bic
072 7# - SUBJECT CATEGORY CODE
Subject category code MBGR1
Source bic
072 7# - SUBJECT CATEGORY CODE
Subject category code PBT
Source bic
072 7# - SUBJECT CATEGORY CODE
Subject category code MAT029000
Source bisac
072 7# - SUBJECT CATEGORY CODE
Subject category code MED071000
Source bisac
072 7# - SUBJECT CATEGORY CODE
Subject category code 615.50724
Source bisac
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Scott Evans
245 10 - TITLE STATEMENT
Title Fundamental Concepts for New Clinical Trialists
250 ## - EDITION STATEMENT
Edition statement 1
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Chapman and Hall/CRC
Date of publication, distribution, etc. 20210331
300 ## - PHYSICAL DESCRIPTION
Extent 348 p
520 ## - SUMMARY, ETC.
Expansion of summary note Fundamental Concepts for New Clinical Trialists describes the core scientific concepts of designing, data monitoring, analyzing, and reporting clinical trials as well as the practical aspects of trials not typically discussed in statistical methodology textbooks. The first section of the book provides background information about clinical trials. It defines and compares clinical trials to other types of research studies and discusses clinical trial phases, registration, the protocol document, ethical issues, product development, and regulatory processes. It also includes a special chapter outlining the valuable attributes that statisticians can develop to maximize their contributions to a clinical trial. The second section examines scientific issues faced in each progressive step of a clinical trial. It covers issues in trial design, such as randomization, blinding, control-group selection, endpoint selection, superiority versus noninferiority, and parallel group versus crossover designs; data monitoring; analyses of efficacy, safety, and benefit-risk; and the reporting/publication of clinical trial results. As clinical trials remain the gold standard research studies for evaluating the effects of a medical intervention, newcomers to the field must have a fundamental understanding of the concepts to tackle real-world issues in all stages of trials. Drawing on their experiences in academia and industry, the authors provide a foundation for understanding the fundamental concepts necessary for working in clinical trials.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Naitee Ting
Relationship A01

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