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