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1-6 of 6 Products & Services

  • Pharmacovigilance
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    Pharmacovigilance (PV)

    PV
    Our innovative solution for Pharmacovigilance replaces the reporting out of safety systems that leverage standard BI tools, breaking the query, wait, evaluate cycle.
  • Signals Medical Review
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    PerkinElmer Signals Medical Review

    SMR

    Built for medical monitors, developed for subject safety, loved by IT. PerkinElmer Signals™ Medical Review empowers medical monitors to detect safety signals faster and reduce time to submission by combining innovative medical data review workflow with advanced analytics. All this on a secure cloud infrastructure.

    Medical monitors need to:

    • Easily find subjects of interest
    • Quickly gain insights using powerful analytics
    • Efficiently track their review progress
     

  • Clinical Outcomes
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    Real-World Evidence (RWE)

    RealWorldEvidence
    Real-World Evidence (RWE) has become an integral component of drug and medical device development, as well as of Health Economics & Outcomes Research (HEOR). Serving as a complement to conventional randomized clinical trials (RCTs), Real-World Evidence collects supporting outcomes and safety data beyond RCTs, that provide a more comprehensive view of a product's real-life therapeutic and economic value to patients, payers, providers and sponsors. With the right data and analytics support, Real-World Evidence informs a common understanding of a drug or device efficacy and safety profile that is used by multiple healthcare stakeholders to drive decisions.
  • Portfolio Management
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    Clinical Portfolio Management

    PortfolioManagement
    Our analytics solutions help companies find the balance between the clinical studies portfolio, resources and budget.
  • Risk Based Monitoring
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    Risk-Based Monitoring (RBM)

    RBM

    Our Risk-Based Monitoring Solution is the most effective way to leverage data-driven insights to optimize site performance while improving patient safety.

    With our solution for risk-based monitoring, the effort spent on complete source-data verification can be significantly reduced. The resulting savings (in both time and costs) allows for better data analysis and better protection of subjects without multiplying costs.

    Benefits of Risk-Based Monitoring include

    • Quickly identify and track actions for high risk sites
    • Reduce complexity by supporting multiple trial designs and data sources
    • Optimize monitoring using adaptive risk models applied to historical study data
  • Clinical Operations
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    Clinical Operations

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