Empower Life Sciences & Pharma with Intelligent AI Automation
Accelerate research, ensure compliance, and unlock real-world insights with AI built for the future of healthcare innovation.
Life sciences and pharmaceutical organizations face increasing demands: regulatory complexity, rising R&D costs, and the need for real-world evidence. Carevyn enables smarter, faster decision-making through automation, advanced analytics, and compliant workflows that power research, trials, and commercialization.
Innovation FocusedDriving Innovation with Data & Automation
Accelerating Clinical Trials
- ✓30% faster data capture across trial sites
- ✓40% reduction in manual reporting tasks
- ✓Fewer protocol deviations with automated compliance tracking
Unlocking Real-World Evidence (RWE)
- ✓Aggregate multi-source patient data securely
- ✓Deliver real-time population health analytics
- ✓Improve drug safety monitoring by 20%
Optimizing Market Access & Reimbursement
- ✓15% faster market access submissions
- ✓Stronger evidence packages with AI-driven analytics
- ✓Higher payer acceptance rates for coverage decisions
Enhancing Pharmacovigilance & Compliance
- ✓Real-time adverse event detection
- ✓Automated reporting to regulators (FDA, EMA)
- ✓SOC 2 + HIPAA-compliant platform for global data security
Seamless Research Platform Integrations
Carevyn transforms clinical documentation and research data capture for life sciences organizations through intelligent automation and regulatory-compliant workflows.
Research Platform Capabilities
- ✓Integrates with clinical trial management systems
- ✓FDA, EMA, HIPAA, SOC 2 compliant security
- ✓Real-world evidence data aggregation
- ✓Scalable across global pharmaceutical operations
- ✓Automated clinical data abstraction and coding
- ✓Real-time adverse event reporting and monitoring
"Accelerate clinical trials with 85% reduction in data capture time."
Why Life Sciences & Pharma Choose Carevyn
30% Faster Trials
Accelerate R&D timelines with AI automation.
20% Improved Drug Safety Monitoring
Proactive pharmacovigilance and real-time analytics.
15% Faster Market Access Submissions
Stronger payer evidence and faster approvals.
40% Less Manual Reporting
Reduce operational burden and errors.
Regulatory-Ready & Secure
FDA, EMA, HIPAA, SOC 2 compliance for global data.
Ready to Power the Future of Healthcare?
Carevyn empowers life sciences and pharma companies to accelerate research, ensure compliance, and unlock patient insights that drive innovation.