Our Work: Stage of Development
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Active
Work underway to develop and launch new resources and solutions
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Embedded Pragmatic Clinical Trials
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Enabling Translational Safety
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Historical Trial Data Sharing
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Interpretation of Clinical Guidances & Regulations
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Modernizing Clinical Trial Conduct
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Modernizing ICSR Management
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Optimizing Data Collection
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Established
Launched work being shared and promoted for adoption across the ecosystem
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Diversity of Participants in Clinical Trials
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Interpretation of Pharmacovigilance Guidances & Regulations
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Site Qualification and Training
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Completed
Work that has concluded, with resources still available for continued use
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Advancing Safety Analytics
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Clinical Data Transparency
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Clinical Research Access & Information Exchange
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Clinical Research Awareness
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Common Serious Adverse Events (SAE) Fields
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Data Monitoring Committee
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Intelligent Automation Opportunities in Pharmacovigilance
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Modernization of Statistical Analytics
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Operationalizing Platform Trials
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Pharmacovigilance Agreements Optimization
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Privacy Methodology for Data Sharing
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Quality Management System
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Rapid Signal Assessment Using Real World Data
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Shared Investigator Platform
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Value of Safety Information Data Sources
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