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Practical Guide to Clinical Data Management [Kõva köide]

(Jazz Pharmaceuticals, CA, USA), (Jazz Pharmaceuticals, CA, USA)
  • Formaat: Hardback, 296 pages, kõrgus x laius: 229x152 mm, kaal: 544 g
  • Ilmumisaeg: 31-Jan-1999
  • Kirjastus: Interpharm Press Inc
  • ISBN-10: 1574910434
  • ISBN-13: 9781574910438
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  • Kõva köide
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  • Tasuta tarne
  • Lisa soovinimekirja
  • Formaat: Hardback, 296 pages, kõrgus x laius: 229x152 mm, kaal: 544 g
  • Ilmumisaeg: 31-Jan-1999
  • Kirjastus: Interpharm Press Inc
  • ISBN-10: 1574910434
  • ISBN-13: 9781574910438
Teised raamatud teemal:
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:
    PART I: ELEMENTS OF THE PROCESS
    Data Management Plan
    Study Setup
    Creating Reports & Transferring Data
    Entering Data
    Managing Lab
    Coding Reported Terms
    Collecting Adverse Event Data
    Closing Studies
    Identifying & Managing Discrepancies
    Tracking CRF Data
    PART II: CDM SYSTEMS
    Where Systems Come From
    System Validation
    Choosing Vendor Products
    Test Plans
    Implementing New Systems
    Migrating Legacy Data
    Change Control
    PART III: SPECIAL TOPICS
    Creating Data Standards
    SOPs & Guidelines
    Working With CROs
    Autocoder Algorithms
    CRF Design Considerations
    Remote Data Entry
    APPENDICES
    Outlines - Data Management Plan
    Database Design Document
    Implementation Plan; Validation Plan
    Test Plan
    GLOSSARY
    SELECTED READING
    INDEX