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Registries for Evaluating Patient Outcomes: A User's Guide

Read the latest news on regulatory-grade real-world evidence: Registries for Evaluating Patient Outcomes: A User's Guide.

Contents

Pre Content

  1. Chapter 1: Patient Registries

  2. Chapter 2: Planning a Registry

  3. Chapter 3: Registry Design

  4. Chapter 4: Selecting and Defining Outcome Measures for Registries

  5. Chapter 5: Data Elements for Registries

  6. Chapter 6: Data Sources for Registries

  7. Chapter 7: Principles of Registry Ethics, Data Ownership, and Privacy

  8. Chapter 8: Informed Consent

  9. Chapter 9: Registry Governance

  10. Chapter 10: Recruiting and Retaining Participants in the Registry

  11. Chapter 11: Obtaining Data and Quality Assurance

  12. Chapter 12: Adverse Event Detection, Processing, and Reporting

  13. Chapter 13: Analysis, Interpretation, and Reporting of Registry Data To Evaluate Outcomes

  14. Chapter 14: Assessing Quality

  15. Contributors and Reviewers

  16. Appendix A: An Illustration of Sample Size Calculations

  17. Appendix B: Copyright Law