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January 13, 2003 | The IT department developed an information structure to centralize the drug development process in a single database system, and then integrated other key components for information sharing and reporting.

Management Reporting
Executive Reporting
Financials
Forecasting
Resource Planning
Strategic Planning
IMS
Drug Development
Resourcing
Clinical Trials
Regulatory
Investigators
Drug Trial Sites
Patient Enrollment
Randomization
Clinical Trial Materials
Monitoring Visits
Document Management
FDA Submissions
Protocols
Amendments
Publications
IRB Documents
Audit Certificates
Investigator Documents
Clinical Data/Safety Data
Patient Safety Data
Case Report Forms
Adverse Event Reports
Statistical Analysis
Finance & Accounting
Payroll
Fixed Assets
HR
Budgets

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