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CROs that leverage the power of PerkinElmer’s advanced analytics solutions for clinical research can effectively support their sponsors’ aggressive drug development timelines while improving operational efficiencies. With our extensive expertise, CROs can feel confident knowing that they are working with informatics professionals delivering solutions to support ICH E6 (R2) guideline compliance.
Aggregate and enrich clinical data from disparate sources quickly and easily
Gain actionable insights from real-time data across the various phases of clinical development
Empower clinical teams to get to the right data faster with guided workflows and self-service data discovery spanning clinical data review (CDR), clinical operations, risk-based monitoring (RBM), safety review (PV) and more
Leverage the power of predictive analytics as trials become larger and more complex by gathering and visualizing data to make smarter decisions earlier
Reveal data insights that contribute to enhanced trial safety measures, streamlined clinical development and support faster launches
Improve subject protection, operational efficiency and data quality while significantly reducing trial costs by decreasing or eliminating wasteful Source Data Verification (SDV).
It is the customer’s responsibility to validate and implement TIBCO Spotfire® software in accordance with their policies and standard operating procedures to ensure compliance with applicable regulations.
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