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Practical Guide to Clinical Data Management

Buch | Hardcover
296 Seiten
1999
Interpharm Press Inc (Verlag)
978-1-57491-043-8 (ISBN)
179,55 inkl. MwSt
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Presents a basic understanding of the role of data management in clinical trials and includes topics such as CDM systems, SOPs, and quality assurance. This book helps you ensure GCP, manage laboratory data, and deal with the kinds of clinical data that can cause difficulties in database applications.
Clinical data management (CDM) has changed from being an essentially clerical task in the late 1970s and early 1980s to a highly computerized, highly specialized field today. And clinical data manages have had to adapt their data management systems and processes accordingly. Practical Guide to Clinical Data Management steers you through a basic understanding of the role of data management in clinical trials and includes more advanced topics such as CDM systems, SOPs, and quality assurance. This book helps you ensure GCP, manage laboratory data, and deal with the kinds of clinical data that can cause difficulties in database applications.

With the tools this book provides, you'll learn how to:

Ensure that your DMB system is in compliance with federal regulations

Build a strategic data management and databsing plan

Track and record CRFs

Deal with problem data, adverse event data, and legacy data

Manage and store lab data

Identify and manage discrepancies

Ensure quality control over reports

Choose a CDM system that is right for your company

Create and implement a system validation plan and process

Set up and enforce data collection standards

Develop test plans and change control systems

This book is your guide to finding the most successful and practical options for effective clinical data management.

include:
ELEMENTS OF THE PROCESS
Data Management Plan
Study Setup
Tracking CRF Data
Entering Data
Managing Lab Data
Identifying and Managing Discrepancies
Collecting Adverse Event Data
Coding Reported Terms
Creating Reports and Transferring Data
Closing Studies
Identifying & Managing Discrepancies

CDM SYSTEMS
Where Systems Come From
Choosing Vendor Products
Implementing New Systems
Systems Validation
Test Plans
Migrating Legacy Data
Change Control

SPECIAL TOPICS
Creating Data Standards
SOPs and Guidelines
Working With CROs
CRF Design Considerations
Remote Data Entry
Autocoder Algorithms

APPENDICES
Appendix A: Data Management Plan Outline
Appendix B: Database Design Document Outline
Appendix C: Validation Plan Outline
Appendix D: Test Plan Outline

GLOSSARY
SELECTED READING
INDEX

Erscheint lt. Verlag 31.1.1999
Verlagsort London
Sprache englisch
Maße 152 x 229 mm
Gewicht 544 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Pharmakologie / Pharmakotherapie
ISBN-10 1-57491-043-4 / 1574910434
ISBN-13 978-1-57491-043-8 / 9781574910438
Zustand Neuware
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