The Resource Clinical Research Informatics, edited by Rachel Richesson, James E. Andrews, (electronic resource)

Clinical Research Informatics, edited by Rachel Richesson, James E. Andrews, (electronic resource)

Label
Clinical Research Informatics
Title
Clinical Research Informatics
Statement of responsibility
edited by Rachel Richesson, James E. Andrews
Contributor
Editor
Editor
Subject
Language
  • eng
  • eng
Summary
Clinical research informatics (CRI) is the application of informatics principles and techniques to support the spectrum of activities and business processes that instantiate clinical research. Informatics, defined generally as the intersection of information and computer science with a health-related discipline, has a foundation drawn from many well-established, theory-based disciplines, including computer science, library and information science, cognitive science, psychology, and sociology. The newly articulated yet fundamental theorem of informatics states that information technology should be used to enable humans to function and perform better together than humans alone, and so informatics is a source for supportive technologies and tools that enhance – but not replace – unreservedly human processes. Clinical Research Informatics contributes to the ongoing dialogues among researchers and practitioners in CRI as they continue to rise to the challenges of a dynamic and evolving clinical research environment. The development of CRI as a sub-discipline of informatics, and as an independent/maturing professional practice area in its own right, drives a growing pool of scientific literature based on original CRI research, and high-impact tools and systems will be developed. CRI leaders and stakeholder groups will continue to support and create communities of discourse that will address much needed practice standards in CRI, improved safety and efficiencies in clinical research, data standards in clinical research, policy issues, educational standards and instructional resources. The Editors and contributors to this book are among the most active and engaged in the CRI domain and provide an excellent primer for deeper explorations into this emerging discipline. Certain themes are highlighted, including the changing role of the consumer, movement toward transparency, growing needs for global coordination and cooperation on many levels, and the merging together of clinical care delivery and research as part of a changing paradigm in global healthcare delivery – all in the context of rapid innovations in technology and explosions of data sources, types, and volume. This book is therefore of considerable interest to all students of biomedical informatics, from the newcomer to the professional informatician
Member of
Is Subseries of
Dewey number
610.28
http://bibfra.me/vocab/relation/httpidlocgovvocabularyrelatorsedt
  • k4VrC0FEHxY
  • dDz_ZdJuCK4
Language note
English
LC call number
R858-859.7
Literary form
non fiction
Nature of contents
dictionaries
http://library.link/vocab/relatedWorkOrContributorName
  • Richesson, Rachel.
  • Andrews, James E.
Series statement
Health Informatics,
http://library.link/vocab/subjectName
  • Medical records
  • Practice of medicine
  • Medical laboratories
  • Health Informatics
  • Health Administration
  • Laboratory Medicine
Label
Clinical Research Informatics, edited by Rachel Richesson, James E. Andrews, (electronic resource)
Instantiates
Publication
Note
Description based upon print version of record
Bibliography note
Includes bibliographical references and index
Carrier category
online resource
Carrier category code
cr
Content category
text
Content type code
txt
Contents
Section I: Contexts of Clinical Research Informatics -- Introduction to Clinical Research Informatics -- From Notations to Data: The Digital Transformation of Clinical Research -- Clinical Research Environment. - Statistical and Study Design Foundations of Clinical Research -- Informatics Approaches to Participant Recruitment -- The Evolving Role of Consumers -- Clinical Research in the Post-Genomic Era -- Section II: Data Management and Systems in Clinical Research -- Clinical Research Information Systems -- Study Protocol Representation -- Data Quality in Clinical Research -- Patient-Reported Outcome Data -- Biobanking Challenges and Informatics Opportunities -- Patient Registries -- Section III: Knowledge Representation and Discovery -- Knowledge Representation and Ontologies -- Non-hypothesis Driven Research: Data Mining and Knowledge Discovery -- Natural Language Processing, Electronic Health Records, and Clinical Research -- Section IV: The Future of Clinical Research, Health, and Clinical Research Informatics -- Data Sharing: Electronic Health Records and Research Interoperability -- Standards Development and the Future of Research Data Sources, Interoperability, and Exchange -- Pharmacovigilance -- Clinical Trials Registries and Results Databases -- Future Directions in Clinical Research Informatics -- Index
Dimensions
unknown
Edition
1st ed. 2012.
Extent
1 online resource (414 p.)
Form of item
online
Isbn
9786613710116
Media category
computer
Media type code
c
Other control number
10.1007/978-1-84882-448-5
Specific material designation
remote
System control number
  • (CKB)3400000000026046
  • (EBL)884452
  • (OCoLC)783118261
  • (SSID)ssj0000850072
  • (PQKBManifestationID)11494572
  • (PQKBTitleCode)TC0000850072
  • (PQKBWorkID)10824852
  • (PQKB)10162585
  • (SSID)ssj0000633406
  • (PQKBManifestationID)11463201
  • (PQKBTitleCode)TC0000633406
  • (PQKBWorkID)10620890
  • (PQKB)10981658
  • (DE-He213)978-1-84882-448-5
  • (MiAaPQ)EBC884452
  • (EXLCZ)993400000000026046
Label
Clinical Research Informatics, edited by Rachel Richesson, James E. Andrews, (electronic resource)
Publication
Note
Description based upon print version of record
Bibliography note
Includes bibliographical references and index
Carrier category
online resource
Carrier category code
cr
Content category
text
Content type code
txt
Contents
Section I: Contexts of Clinical Research Informatics -- Introduction to Clinical Research Informatics -- From Notations to Data: The Digital Transformation of Clinical Research -- Clinical Research Environment. - Statistical and Study Design Foundations of Clinical Research -- Informatics Approaches to Participant Recruitment -- The Evolving Role of Consumers -- Clinical Research in the Post-Genomic Era -- Section II: Data Management and Systems in Clinical Research -- Clinical Research Information Systems -- Study Protocol Representation -- Data Quality in Clinical Research -- Patient-Reported Outcome Data -- Biobanking Challenges and Informatics Opportunities -- Patient Registries -- Section III: Knowledge Representation and Discovery -- Knowledge Representation and Ontologies -- Non-hypothesis Driven Research: Data Mining and Knowledge Discovery -- Natural Language Processing, Electronic Health Records, and Clinical Research -- Section IV: The Future of Clinical Research, Health, and Clinical Research Informatics -- Data Sharing: Electronic Health Records and Research Interoperability -- Standards Development and the Future of Research Data Sources, Interoperability, and Exchange -- Pharmacovigilance -- Clinical Trials Registries and Results Databases -- Future Directions in Clinical Research Informatics -- Index
Dimensions
unknown
Edition
1st ed. 2012.
Extent
1 online resource (414 p.)
Form of item
online
Isbn
9786613710116
Media category
computer
Media type code
c
Other control number
10.1007/978-1-84882-448-5
Specific material designation
remote
System control number
  • (CKB)3400000000026046
  • (EBL)884452
  • (OCoLC)783118261
  • (SSID)ssj0000850072
  • (PQKBManifestationID)11494572
  • (PQKBTitleCode)TC0000850072
  • (PQKBWorkID)10824852
  • (PQKB)10162585
  • (SSID)ssj0000633406
  • (PQKBManifestationID)11463201
  • (PQKBTitleCode)TC0000633406
  • (PQKBWorkID)10620890
  • (PQKB)10981658
  • (DE-He213)978-1-84882-448-5
  • (MiAaPQ)EBC884452
  • (EXLCZ)993400000000026046

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