ORP Manual
Table of Contents
Appendices
Introduction
Appendix A: Abbreviations
Chapter 1: Audits
Appendix B: ORP Organizations
Chapter 2: Clinical Trials Concept
Appendix C: ORP Roster Link and Roster Update Form
Chapter 3: Cooperative Group Concept
Appendix D: Clinical Training Sessions
Chapter 4: Data Submission
Appendix E: Technical References and Formulas
Chapter 5: Discipline Review
Chapter 6: Drug Ordering and Maintenance
Chapter 7: Ethical and Regulatory Considerations
Chapter 8: Expectation Report and IPR
Chapter 9: Intergroup Studies
Chapter 10: Long Term Follow Up
Chapter 11: Response Assessment
Chapter 11a: Response Assessment-Leukemia
Chapter 11b: Response Assessment-Lymphoma
Chapter 11c: Response Assessment–Myeloma
Chapter 12: Registering a Patient
Chapter 13: Serious Adverse Events
Chapter 14: Study Protocol
Chapter 15: Adverse Event Assessments
Chapter 16: General Forms and Guidelines
Chapter 16a: General Forms and Guidelines-Leukemia Forms
Chapter 16b: General Forms and Guidelines-Lung Forms
Chapter 16c: General Forms and Guidelines-Lymphoma Forms
Chapter 16d: General Forms and Guidelines-Myeloma Forms
Chapter 16e: General Forms and Guidelines-S1400 & Sub-Studies
Chapter 16f: General Forms and Guidelines- S1404 Forms and Specimens
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