Registries

Gain Real-World Insight and Get Clarity Now!

Registries represent a unique and powerful model for the collection of observational, epidemiologic, health management, economic and other outcomes data. This study model is used to accelerate innovation, produce faster knowledge gains and alert companies to potential problems with their products. They are not clinical trials and therefore, should not be conducted like clinical trials.

Clinipace Worldwide has extensive registry experience and know how to right-size your registry by deploying appropriate technology to perfectly meet your registry needs. This eliminates bloat while giving you the Right-Sized™ services to deploy your registry.

Powerful Enough for Clinical Trials Yet Perfect for Registries

Clinipace Worldwide provides your organization with technology-driven services sophisticated enough to run clinical trials but flexible enough to support your registry. As a result you get the most advanced scientifically rigorous registry platform, yet all the power of real-time visibility, reporting, and site management.

Examples of how customers have engaged Clinipace Worldwide for their registry projects:

  • Patient safety
  • Drug utilization and effectiveness
  • Post-marketing surveillance
  • Prospective product surveillance and risk mitigation
  • Disease progression
  • Quality improvement initiatives
  • Patient population dynamics
  • Provider outcome
  • Relationship building with physicians and patients


Commitment to Clean Data and Clear Decisions

The success of registries is largely determined by investigator or contributor participation. The more sites that participate, the more data that can be collected and the better your insight. Our technology, TEMPO™ is designed to be easy-to-use and to scale across a large investigator base with very little training required. By reducing the impact on the practice, TEMPO will yield better investigator participation rates while delivering:

  • Simple and quick data collection
  • Protocol compliance
  • Data quality and query management
  • Real-time reporting engine
  • Milestone-driven payment
  • Increased accuracy
  • Adverse event reporting


Right-Sized™ Registry Services

Clinipace Worldwide has extensive experience in conducting registries and know how to balance the needs of sponsors and investigators by providing the complete service infrastructure to support each project’s needs.

Clinipace Worldwide technology (EDC/ePRO) provides:

  • Complete visibility into all aspects of your registry
  • Registry set-up and support
  • Data collection and project management tools
  • Powerful reporting engine
  • Robust data validation and management
  • Centralized, remote monitoring
  • Workflow management
  • Audit trail
  • eSignature

Clinipace Worldwide Service Delivers...

Project Management

  • Technology set-up & implementation
  • Good Clinical Practice Adherence
  • Comprehensive project plan
  • Site coordination
  • Project lifecycle management
  • EDC best practices
  • Training

Central Monitoring

  • Ensure informed consent
  • Complete site management
  • Review study files for completeness
  • Query resolution
  • eCRF review
  • Identify AE/SAE

Data Management

  • Data validation and cleansing
  • Quality assurance
  • Manage audit database
  • Medical/Clinical coding
  • Project-specific data dictionaries
  • Third-party data reconciliation
  • Biostat preparation

Biostatistical Services

  • Statistical support for study design
  • Consult on randomization methodology
  • Detailed statistical analysis
  • Real-time reporting
  • Documentation
  • Production of tables, listing & figures
  • Support for manuscripts & abstracts