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