Join Princeton Blue at SCOPE 2026

Visit Booth 1522 to explore how Intelligent Process Automation and connected clinical workflows can help your teams

Feb 2-5, 2026

Orlando, FL

Booth 1522

PB SCOPE 2026
appian life sciences forum header light

Network, exchange ideas, and collaborate with your peers from the pharmaceutical industry.

November 11, 2025

Regeneron Pharmaceuticals,
Tarrytown, NY

We are thrilled to be part of the 2025 Appian Life Sciences Forum. Join us to uncover how AI and Process Automation are reshaping the way life sciences organizations work.

Event Highlights

  • A leading forum for clinical operations excellence with hundreds of sessions, panel discussions, and strategic conversations across every stage of the clinical trial process
  • A global community of 4,500+ attendees representing pharma, biotech, CROs, technology innovators, and research sites from over 30 countries
  • Focused learning and real-world insights delivered through keynotes, fireside conversations, and cross-functional panels that highlight both strategic direction and hands-on practices

Why Attend (and Visit Booth 1522)

  • See how we help clinical operations teams reduce manual effort, gain real-time visibility, and bring greater consistency to study start-up and execution.
  • Meet our experts to discuss how you can streamline study feasibility and site selection, connect data across systems, and leverage AI for clearer, faster decisions. Discuss your use cases with our experts.
  • Bring a current operational challenge, and we’ll walk through how automation and workflow orchestration can simplify it.

Agenda and Registration

Appian Solutions for Life Sciences

Princeton Blue Innovation Lab focuses exclusively on delivering Process Automation solutions for the Life Sciences industry, so you can focus on bringing drugs to market faster. With AI powering these solutions, you can bring scale, efficiency and profitability to your operations faster.

Our Experience in Life Sciences

Princeton Blue is a trusted leader in Process Automation to deliver business outcomes in weeks for Pharmaceuticals, Biotech, and Medical Device clients. Using the Appian AI process platform, our solutions automate workflow, integrate data from your systems like Veeva, Oracle, SAP, and more, to deliver actionable intelligence. In our 16-year Appian partnership, we have supported 13 global Life Sciences clients with projects across Clinical, Regulatory, Lab, and Manufacturing. Leverage our expertise in Life Sciences and Appian to accelerate your process transformation journey.

Projects Delivered Graph Dec 2025

Using Low-Code Automation to Manage the Clinical Supply Chain

See how workflow automation and data integration across siloed systems helped Merck drive significant value.

Hear from Merck on Clinical Automation

Mercks shares its automation journey around managing change in Clinical Data Management with Appian and Princeton Blue.

Projects Delivered

Clinical

Protocol Activity Schedule

Patient Eligibility

Clinical Supplies Job Readiness

Clinical Supplies Scheduling Tool

Study and Site Feasibility

Site Contact Information

Real-World Evidence

Monitoring Visit Report

User Access Management

Study Start-up

Clinical Planning

Standards Request Workflow

Patient Engagement Management

Integrated Evidence Planning

Clinical Complaint Management

Clinical Identity Access Management

Manufacturing

Asset Disposal

Temperature Excursion

Regulatory

EU Clinical Trials Regulation

Label Change Workflow

Dossier Change Control

Health Authority Correspondence

Regulatory Submission Planning

Regulatory Information Management

Lab

Lab Experiment Automation

Lifecycle Management

Lab Shared Services Request Processing

Medical Devices

Personalized Surgical Planning and Implementation

Regulatory Information Management

below proj v2

Clinical

Protocol Activity Schedule

Patient Eligibility

Clinical Supplies Job Readiness

Clinical Supplies Scheduling Tool

Study and Site Feasibility

Site Contact Information

Real-World Evidence

Monitoring Visit Report

User Access Management

Study Start-up

Clinical Planning

Standards Request Workflow

Patient Engagement Management

Integrated Evidence Planning

Clinical Complaint Management

Clinical Identity Access Management

Regulatory

EU Clinical Trials Regulation

Label Change Workflow

Dossier Change Control

Health Authority Correspondence

Regulatory Submission Planning

Regulatory Information Management

Lab

Lab Experiment Automation

Lifecycle Management

Lab Shared Services Request Processing

Medical Devices

Personalized Surgical Planning and Implementation

Regulatory Information Management

Explore Resources

Here are some insights to help in your research journey

Why Faster Clinical Trials Need More Than Automation The Role of AI in Clinical Execution Blog Feature 2

Why Faster Clinical Trials Need More Than Automation: The Role of AI in Clinical Execution

Consider this scenario. A clinical study is underway. Enrollment is progressing, sites are active, and dashboards suggest things are broadly on track. Now imagine being ...
Read more
Accelerating Regulatory Submissions How AI Agents are Eliminating the Last Mile of Manual Work in Pharma R D Blog Feature

Accelerating Regulatory Submissions — How AI Agents are Eliminating the Last Mile of Manual Work in Pharma R&D

Pharma R&D is entering a new phase of acceleration. As development pipelines expand and submission volumes increase, organizations are placing greater focus on the operational ...
Read more
The True Cost of Delays in Clinical and Regulatory Operations and How to Reduce It Feature

The True Cost of Delays in Clinical and Regulatory Operations – and How to Reduce It

In most pharma and biotech organizations, delays in clinical trials, regulatory submissions, and overall drug development timelines are rarely surprising. They tend to show up ...
Read more
Scroll to Top