The objective of this study is the development, implementation and management of a registry of patient data that captures clinically meaningful, real-world, data on the diagnosis, nature, course of infection, treatment(s) and outcomes in patients with complex disease globally.
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Assess Natural history
Timeframe: 5 years
Assess Clinical, Cost and/or Comparative Effectiveness
Timeframe: 5 years
Assess Safety
Timeframe: 5 years
Measuring and/or Improving Quality of Care
Timeframe: 5 years