Pan-African Clinical Research Network (Hub & Spoke Architecture)
Connecting centralized academic tertiary research hospitals to community health center spokes where patients receive primary care.
Select a site to inspect capability
Click any clinical site node on the left to review investigator capacity, cold-chain readiness, biobanking specs, and linked spoke clinics.
RFP Feasibility & Protocol Matching Engine
Rapid turnaround feasibility assessment for international pharmaceutical sponsors and CRO development partners.
Protocol Requirements (Sponsor Input)
Feasibility Evaluation Output
Configure protocol parameters and click generate to assess network capacity and enrollment velocity.
Offline-First eSource & Mobile Clinic Encounter Simulator
Built for primary clinic coordinators operating in rural and intermittent connectivity environments. 21 CFR Part 11 ALCOA+ audit compliant.
Spoke Clinic Patient Encounter Entry
Online QueueVerified eSource Log (Audit Trail)
SHA-256 VerifiedParticipant Engagement, Multilingual Nudges & Automated Stipends
Driving EzCRO's industry-leading 85–96% retention rate with cultural engagement and instant mobile money reimbursements.
Automated Multilingual Protocol Nudges
WhatsApp / SMS GatewayInstant Participant Transport Stipend Disbursals
Ozow / Mobile Money IntegrationTransport stipends are automatically triggered upon nurse check-in at primary care spoke clinics, eliminating cash handling risks on site.
Sentinel Outbreak & Pandemic Preparedness Surveillance Console
Powers EzCRO's Service 03. Standing research infrastructure capable of 72-hour trial surge activation for emerging pathogens.
STANDING SURVEILLANCE & EARLY SIGNAL DETECT
When an outbreak signal exceeds baseline thresholds, EzCRO’s standing ethics frameworks, cold-chain pipelines, and pre-trained investigator network can activate Phase I-IV vaccine and therapeutic trials in 72 hours.
Sentinel Primary Care Node Surveillance Feed
Real-time Syndromic Feed| Node & Site | Syndromic Indicator | Weekly Volume | Baseline Deviation | Signal Status | Last Update |
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Regulatory Compliance & Inspection-Ready eTMF
Continuous alignment with SAHPRA (South Africa), African Medicines Agency (AMA), ICH-GCP E6(R2/R3), and FDA 21 CFR Part 11.
SAHPRA Milestone Tracker
- Protocol Submission Completed Day 0
- Ethics Review (NHREC Accredited) Approved (Week 4.8)
- IMP Import Permit Verification Under Review (ETA 3 Days)
- First Patient In (FPI) Target Target: ≤ 7 Days post-clearance
ALCOA+ Data Integrity Standard
- ✅ Attributable: Cryptographic digital sign-offs by GCP staff.
- ✅ Legible: Native digital source records, zero transcription loss.
- ✅ Contemporaneous: Real-time timestamping at patient visit.
- ✅ Original: Primary digital capture at spoke nodes.
- ✅ Accurate: Automated sanity limits on vitals and eligibility.