Join us at Booth 1807
Meet our Appian experts at Booth #1807 and ask us about solutions for Clinical, Regulatory, Lab and Medical Devices.
Princeton Blue is proud to be a sponsor again at DIA Global 2025. If you’re in attendance, we invite you to visit us at Booth 1807. Ask us about solutions to streamline and automate critical business workflows in Clinical, Regulatory, Lab and Medical Devices.
Our Experience in Life Sciences
Princeton Blue is a trusted leader in AI-powered process automation for pharmaceutical and biotech clients using Appian’s Low-code technology to deliver business outcomes in weeks.
We develop advanced workflow solutions that use Data Fabric to augment your existing systems such as Veeva, SAP and LIMS/ELN, and present a unified view of your enterprise data, use Private AI to turn that data into actionable intelligence, to deliver process automation across use cases in Clinical, Regulatory, Lab, and Manufacturing.
Princeton Blue is recognized by leading industry analysts for deep expertise Low-code technologies and decades of work experience in the Life Sciences industry. Some of the world’s largest pharmaceutical and biotech companies trust us to automate and intelligently transform their most strategic drug development processes. Let’s work together to accelerate your digital transformation journey.
Build an Appian POC
Leverage our Deep Appian Expertise
Princeton Blue has been a trusted Appian partner for 16 years, and during that time, we have had 370 Appian project releases for our Pharma and Biotech customers.
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
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.
Appian Solutions for Life Sciences
Real-World Evidence
Establish a flexible workflow, monitor milestones, enhance collaboration, and gain valuable insights into study execution.
Clinical Complaint Management
Streamline incoming clinical complaint analysis and intake with Gen AI, empowering faster human resolution.
Labeling
Streamline global label changes with real-time visibility and country-specific workflow customization using Appian’s Case Management Studio.
EU-CTR
Streamline and automate the internal workflow process for regulatory submission/transition under the new EU-CTR guidelines.
Regulatory Submissions
Orchestrate the entire workflow from document identification to approvals to submission.
Clinical Supplies Shipping
Integrate clinical supply systems, automate workflows, and deliver a rich user experience to streamline and automate your clinical supplies shipping process.
Study Data Access Management
Automate the process of user access requests for study data using Low-code and workflow automation.
Study Start-up
Automate the workflow and collaboration of the clinical study start-up process allowing for variations in business rules and regulatory requirements across countries.
Lab Experiment Automation
Leverage Low-code Process Automation to modernize lab operations by augmenting and enhancing your traditional LIMS, ELN and other existing systems.
Drug Safety
Automate the processing of adverse event signals through effectively logging and investigating drug safety issues by leveraging BPM and Low-code.
Build a Proof of Concept
Use our Innovation Lab to build a Proof of Concept before you invest in Appian. Brainstorm with our team of experts and see what works best for you.
This is a very popular service and is used by many of our clients. We have delivered numerous Proof of Concepts for our clients. Contact us if you have a use case in mind and see how our Innovation Lab can help you.
