ADAPT Clinical Trial LMS

Empowering Investigators and Sponsors through a custom-tailored Learning Management System

Bringing a medical device to market takes more than innovation. It requires precision, compliance, and confidence at every stage of the clinical journey. Ensuring every investigator and site team is properly trained and aligned is essential to trial success and regulatory readiness.

This customizable solution empowers your organization to deliver, track, and document each phase of investigator and site training, from protocol development through post-approval education. Built for consistency and accountability, it provides the structure and oversight needed to streamline training, strengthen compliance, and accelerate your path to market.

ADAPT LMS supports your customer education and sales team training needs. Tailored for life science organizations, ADAPT LMS offers your learners exactly what they need when and where they need it. Our learning management system offers flexibility to scale and customize to your specific needs.

Streamlined Study Training

ADAPT centralizes every element of your clinical training program into one unified, validated system. Each phase, Host, Deliver, Track, and Update, is designed for regulatory compliance, version control, and study readiness.

  • Host– Securely upload and manage all GCP, protocol, and device training materials.

  • Deliver – Assign courses by role; enable in-system completion or credit external learning.

  • Track – Monitor progress with interactive dashboards, ensuring full compliance and documentation traceability.

  • Update – Control versioning for evolving protocols, track expirations, and manage retakes automatically.

Performance Gains for Every Stakeholder

You gain acceleration of study activation while reducing the training burden and delivering measurable outcomes for investigators, coordinators, and sponsors alike.

For Sites

  • Faster onboarding and reduced administrative load

  • Clear, role-based training paths

  • Consistent protocol adherence and fewer errors

For Sponsors

  • Reduced protocol deviations and compliance risk

  • Enhanced inspection readiness with real-time dashboards

  • Centralized oversight of training completion and qualifications

Built for Compliance and Validation

Your custom LMS is developed to meet the highest regulatory standards, aligning with FDA and GCP requirements, ensuring confidence from audit to inspection.

  • Secure Electronic Signature

  • “Read & Understood” Acknowledgments

  • Comprehensive Audit Trails

  • Automated Version Control

  • Timestamped Documentation

  • Access Control and Data Security

Ready to learn more about ADAPT Clinical Trial LMS?