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Clinical Operations

Improve subject protection, operational efficiency and data quality while significantly reducing trial costs by decreasing or eliminating wasteful Source Data Verification (SDV).

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Optimize Clinical Development Operations

Leveraging our industry leading risk-based monitoring solution, improved subject protection, operational efficiency and data quality can be achieved. Trial costs can be cut via the reduction in source document verification.


  • Meet study milestones
  • Ensure proper fiscal management and forecasting
  • Enable a pay for performance model with outsourced providers and internal resources

Resources, Events & More

All (14)
Resource Type File Name File Format
Brochure Solutions for Risk-based monitoring PDF  906 KB
Brochure Solutions for Trial Operations PDF  662 KB
Interactive Demo Clinical Data Review Link
Interactive Demo Pharmacovigilance Data Exploration Link
Interactive Demo Pharmacovigilance Reporting Compliance Link
White Paper Clinical Data Aggregation White Paper
White Paper Speeding the Switch to Risk-Based Monitoring White Paper
White Paper The Foundation of Risk-Based Monitoring Success White Paper
White Paper Transforming Clinical Development White Paper
White Paper Real–World Evidence Through Advanced Analytics White Paper
White Paper Achieving Pharmacovigilance Excellence White Paper
White Paper Placing the Patient First White Paper
White Paper Planning Quality into Clinical Trials: Integrating RBM and QbD White Paper
White Paper Achieving Clinical Operations Excellence White Paper