Real-World Evidence
Organize and streamline real-world studies with process automation and AI.
Princeton Blue’s Real-World Evidence (RWE) solution simplifies the organization and tracking of Real World Evidence studies throughout their entire lifecycle. Built on the Appian platform, this solution allows RWE teams to establish a flexible workflow, monitor dynamic milestones, enhance collaboration, and gain valuable insights into study execution.
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Real-World Evidence (RWE) studies are instrumental in providing critical insights. These studies support regulatory approvals, market access, and post-market monitoring.
The Challenges in Real-World Evidence Study Planning
Traditional planning and management of these studies with tools such as Spreadsheets, Word documents, SharePoint and Email add unnecessary complexity, do not have transparency and are a risk from a security perspective.
The following are some challenges encountered when planning RWE studies using traditional methods:
- Time-consuming manual processes requiring extensive documentation across multiple files
- Inconsistent study planning due to lack of standardized templates and workflows
- Limited collaboration when multiple stakeholders need to contribute and review.
- Poor visibility across your portfolio of RWE studies.
- Compliance concerns from inadequate audit trails and version control.
- Administrative burden that takes focus away from scientific and strategic work.
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The Solution
Princeton Blue’s real-world evidence solution combines the power of AI with Appian’s process orchestration to streamline your end-to-end RWE workflow.
The solution simplifies the organization and tracking of Real World Evidence studies throughout their entire lifecycle. Built on the Appian platform, this solution allows RWE teams to establish a flexible workflow, monitor dynamic milestones, enhance collaboration, and gain valuable insights into study execution.

Key Features of the Solution

Simplified User Experience

Flexible Approvals

Dynamic Workflows

AI-powered Analysis

Process Reporting

Fully Customizable
Key Features of the Solution
Process Improvement
- Automation of Part 1 and Part 2 document identification via configurable business rules
- Customizable workflows for defining and approving documents.
- Flexibility to easily make changes to execution parameters such as priorities, owners, due dates, and more, driven by the ever-changing business needs.
Process Monitoring and Compliance
- In-depth insight into the submissions process via interactive graphical dashboards and reports.
- Proactive identification of potential bottlenecks to ensure SLA compliance with active process monitoring.
- Detailed audit-trail for compliance audits and driving accountability.
Integration
- Integration with existing systems to pull and push data as and when needed in the process.
- Automation of document organization with a Document Repository for easy retrieval and offline search.
User Experience
- Intuitive user experience across all devices, form factors and platforms with a mobile-enabled modern design.
- Easily customized and adapted to your needs.