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"Clinical Development" 1-8 of 8 Products and Services

Clinical Data Review

Clinical Data Review (CDR)

The PerkinElmer Clinical Data Review Solution provides the most effective way to perform in-stream review of study data, empowering clinical development teams to make smarter decisions faster.

Our Clinical Data Review solution provides Medical Monitors, Safety Review Teams, Biostatisticians, Data Managers, Pharmacologists, and others challenged with analyzing clinical data with a powerful and advanced analytics solution to overcome clinical data review challenges. The solution enhances medical review workflows, allowing organizations to make more informed decisions on the safety and efficacy of therapeutics earlier in development.

Portfolio Management

Clinical Portfolio Management

Our analytics solutions help companies find the balance between the clinical studies portfolio, resources and budget.
Clinical Outcomes

Real-World Evidence (RWE)

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.

Pharmacovigilance (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 - SMR

Signals Medical Review

PerkinElmer Signals Medical Review empowers medical monitors to detect safety signals faster and reduce overall time to submission by combining innovative medical review workflow with advanced analytics.
  • Single, unified data analytics solution – from source to visualization to action
  • Curated analytics experience with configurable alerts on cohorts of interest
  • 360 degree visibility across CDISC domains with built-in patient profiles
  • Medical Review status reporting and tracking
  • Secure, regulatory compliant cloud solution
  • Visualization and analytics powered by industry-leading TIBCO Spotfire
Risk Based Monitoring

Risk-Based Monitoring (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
Supply Management

Clinical Supply Management

Clinical supply monitoring analytics enable the oversight of packaging, distribution, returns, reconciliation and quality management of clinical kits.
Clinical Operations

Clinical Operations

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

"Clinical Development" 1-8 of 8 Products and Services