Protocol management, adverse event tracking, blinded study management, 21 CFR Part 11 compliance, and multi-site coordination — deployed in weeks, not months.
Audit trail: every action logged
What CROs Need From a CTMS — And What Hekma Delivers
Sync to all sites automatically. Every amendment distributes in minutes — no email chains.
Sites see only their patients and data. Sponsor sees everything. Enforced at every level.
Real-time AE reporting with automated escalation workflows.
Placebo integrity maintained automatically. No accidental unblinding.
Every action logged with immutable audit trail for FDA submissions.
Complete real-time view across all sites from one screen.
License Hekma CTMS and offer to pharma clients as your own platform.
Data sovereignty requirements met. Customer's environment, their control.
Implementation Timeline
| Deployment | Timeline | Best For |
|---|---|---|
| Multi-tenant SaaS | Live in 3–5 business days | SMB pharma, startup biotechs, smaller CROs |
| Private VPC | Live in 4–8 weeks | Large pharma with data sovereignty requirements |
| On-Premises | 8–16 weeks | Federal/regulated environments |
Your branding. Your relationship. Our infrastructure. Offer Hekma CTMS to your pharma clients as your own platform.
Enrollment data from patient identification flows automatically into CTMS. No double-entry. No reconciliation.
60% of SMB CROs still coordinate trials across spreadsheets. This ends that.
Integrations & Compliance
Deploy in days. White-label to your clients. Connected to the patient recruitment layer from day one.