Tech-Enabled Services Include:
The Vicore Health Regulatory Ecosystem
Integrated Intelligence Across RA, PV and Quality
At Vicore Health, we combine deep multi-geography regulatory expertise with advanced automation and AI-driven platforms to strengthen our core capability areas across Regulatory Affairs (RA), Pharmacovigilance (PV), and Quality Assurance (QA).
Each capability is supported by purpose-built technology within our growing product suite.
Life Cycle Management
Lower cost, improved timelines, and strengthened compliance control.
End-to-End Control Across the Product Journey
Managing renewals, variations, submissions, and post-marketing obligations across multiple markets requires structured oversight.
What we enable
- Streamlined lifecycle operations
- Coordinated renewals, variations, and PV integration
- Cross-market submission planning and tracking
Powered by
ARC – Workflow coordination and submission planning support.
Safety (Pharmacovigilance)
Al-enabled literature surveillance that strengthens patient safety while reducing manual workload.
Intelligent, Integrated Safety Monitoring
Pharmacovigilance systems must be compliant, efficient, and scalable, particularly in complex and under-resourced regulatory environments. Al-powered literature surveillance supports safety teams by automating high-volume screening tasks while maintaining rigorous oversight and regulatory alignment.
What we enable
- Al-powered pharmacovigilance literature surveillance
- Automated ingestion and monitoring of global and African scientific publications
- Human-in-the-loop validation to ensure regulatory compliance and signal accuracy
- Structured workflows for adverse event identification and safety reporting
Powered by
LewisLit – Al-powered literature surveillance for automated detection and screening.