A centralized Clinical Trial Management System designed to help CROs manage operational, administrative, and patient-related aspects of clinical research within a unified platform.
Deploy in days. White-label under your brand. Supports study planning, patient tracking, visit management, compliance workflows, and multi-site coordination. Offer it as a service to your pharma clients.
White-label ready
21 CFR Part 11 · BAA included · HIPAA compliant
Managing clinical trials across disconnected tools and manual processes creates operational inefficiencies, compliance risks, and reduced visibility into study progress. CROs need a modern platform they can deploy fast and scale across clients.
Centralises trial operations
Improves workflow coordination
Simplifies patient tracking
Enhances compliance oversight
Reduces administrative complexity
Enables scalable research management
HEKMA CTMS consolidates trial workflows into a single intelligent environment, enabling research teams to manage patient visits, milestones, documentation, and operational activities more efficiently.
“By improving coordination across investigators, coordinators, and departments, CROs gain greater control over trial execution while reducing manual effort and operational fragmentation.”