珀金埃尔默网站上的Cookie
珀金埃尔默使用cookies来确保我们为您提供在我们网站上的最佳体验。 这可能包括来自第三方网站的cookies。 如果您不改变您的设置点击继续,我们会认为您同意接收本网站的cookies。 您可以随时更改您的Cookie设置。 要了解更多信息,请查看我们的Cookie政策,其中包含有关如何管理Cookie的信息。

Clinical CROs

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

Featured Solutions

Clinical Data ReviewClinical Data Review

Anticipate, answer and act on clinical/medical review questions, uncover trends, patterns and risks through self-service discovery.

Risk-Based MonitoringRisk-based Monitoring

Realize significant time reduction spent on physical clinical site inspections while preserving clinical trial data quality.

Clinical OperationsClinical Operations

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

PharmacovigilancePharmacovigilance

Improve ways to work with pharmacovigilance data, find insights and drive operational efficiency.

Real-World EvidenceReal World Evidence

Accelerate time to insight with pre-built analysis modules that create the possibility to conduct an end-to-end analysis in one place.

Portfolio ManagementPortfolio Management

Successfully manage clinical development candidates by finding the balance between the clinical studies portfolio, resources and budget.

Supply ManagementSupply Management

Understand aggregate demand across different protocols for clinical kits to gain an overall demand view at an enterprise level.

Featured Content

 

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.