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http://dx.doi.org/10.1201/9781420037654
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Front MatterAbstract - Hi-Res PDF (535 KB) - PDF w/links (535 KB)
1
Chapter 1. Definitions and ConceptsAbstract - Hi-Res PDF (966 KB) - PDF w/links (827 KB)
25
Chapter 2. Assessing Drug SafetyAbstract - Hi-Res PDF (737 KB) - PDF w/links (613 KB)
39
Chapter 3. International Regulatory PerspectivesAbstract - Hi-Res PDF (1213 KB) - PDF w/links (1119 KB)
61
Chapter 4. Types of Risk in Clinical TrialsAbstract - Hi-Res PDF (686 KB) - PDF w/links (604 KB)
79
Chapter 5. Risk Identification and QuantificationAbstract - Hi-Res PDF (994 KB) - PDF w/links (829 KB)
95
Chapter 6. Threats and OpportunitiesAbstract - Hi-Res PDF (791 KB) - PDF w/links (642 KB)
109
Chapter 7. Planning Preventative StrategiesAbstract - Hi-Res PDF (1081 KB) - PDF w/links (985 KB)
125
Chapter 8. Backup PlanningAbstract - Hi-Res PDF (959 KB) - PDF w/links (784 KB)
143
Chapter 9. Project Tracking and Decision-MakingAbstract - Hi-Res PDF (1172 KB) - PDF w/links (980 KB)
169
Chapter 10. Investigational Site Risk ManagementAbstract - Hi-Res PDF (660 KB) - PDF w/links (628 KB)
187
Chapter 11. Post-Project EvaluationAbstract - Hi-Res PDF (653 KB) - PDF w/links (520 KB)
201
ReferencesAbstract - Hi-Res PDF (277 KB) - PDF w/links (277 KB)
197
ConclusionsAbstract - Hi-Res PDF (269 KB) - PDF w/links (269 KB)
