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Navigate compliance and reduce risks throughout your clinical trial with our experts at your side.
Enhance clinical trial efficiency and power global studies with the industry leader in practical, eClinical innovation. Simplify and automate clinical processes around the world.
Streamline clinical research from site identification to study closeout with seamlessly connected solutions and services that support your success.
Navigate the ever-evolving global regulatory landscape with technology and services that ensure compliance, mitigate risk, and avoid costly delays.
Simplify quality control across your clinical content, processes, and training with scalable and comprehensive quality solutions.
Reduce IT burdens throughout your study with technology that meets usability, scalability, performance, validation, connectivity, and security requirements.
Corrective and Preventive Action (CAPA) management is a cornerstone of quality and compliance, but many CROs and site teams struggle to know where to begin. With the recent updates to GCP guidelines, ICH E6(R3), now is the time to ensure your CAPA process is risk-based...
Library
Blog
The Reality of Long-Term System Integrations in Life Sciences
What 2025 Taught Us About Clinical Trial Complexity and What We Are Taking Into 2026
Webinar
Ask an Expert Office Hours - ICH E6(R3)
Ask an Expert: GlobalLearn (LMS) Site Training
Ask an Expert TMF Office Hours - Culture
Ask an Expert TI Tech Office Hours - Lean Oversight
Auditorías en TMF: Recomendaciones para minimizar hallazgos
Understanding Risk-Based CAPA Under ICH E6(R3)
From Systems to Success: Why Your Tech Partners Must Understand Clinical
MHRA Inspection Insights: ICH E6(R3) and the Next Chapter of Quality
No File Left Behind: The Great TMF Migration to Archive
Quiz
TMF Inspection Risk Score® Survey | Assess in 10 Minutes
eTMF Integration: The Minimum-Viable Flows Between CTMS and eISF
eTMF Integration: Metadata That Moves: Mapping Documents, Training, and Sites Across Systems
How to OpTImize TMF Processing
OpTImize ClinOps: The Power of eTMF & CTMS Integration
Quick Guide
Essential Checklist for eTMF Archiving
Strengthening the Backbone of Clinical Trials: The TMF in a Digital World
Evade Pitfalls and Improve Timelines in Your Study Start-Up
eISF 101: Digitizing Investigator Site Files for Better Compliance, Security, Efficiency
Key Takeaways from OpTImize London
Alleviating CRA Burdens with eClinical Innovation
TMF Mock Inspection & Internal Quality Review Checklist
Preparing for a Regulatory Inspection
