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Beyond Boundaries: How Oryxion Delivers Clinical Data Around the Clock
In clinical research, time isn’t just money it’s momentum.
At Oryxion, we’ve built a delivery model that works while you rest combining local expertise with global execution to accelerate your timelines without compromising quality.
Here’s how we deliver around-the-clock value:
🌐 Time-Zone Advantage: Our India-based delivery hub works in tandem with global sponsors, turning downtime into progress.
✅ Rigorous Oversight: Our senior SMEs and QA teams ensure every deliverable meets the highest regulatory and scientific standards.
📉 Optimized Cost Efficiency: Strategic resourcing enables sponsors to reinvest budget into innovation and growth.
📊 Scalable by Design: From Phase I to multi-region studies, we adapt fast without diluting quality.
Whether you need Clinical Data Management, Statistical Programming, Biostatistics, Medical Writing or Regulatory-ready outputs Oryxion makes it seamless, secure, and scalable.
Accelerate Your Clinical Data Strategy with Oryxion
Slow study builds, disconnected systems, and messy data pipelines shouldn’t hold back your trials. That’s where Oryxion comes in.
We’re a tech-enabled Data CRO purpose-built to streamline clinical data from protocol to submission fast, clean, and connected.
What sets us apart?
We offer an integrated, platform-driven model with end-to-end services, including:
· Clinical Data Management
· Biostatistics & Statistical Programming
· Medical Writing tied directly to your data workflows
· SDTM automation + mapping tools
· AI/ML-powered database build automation
Our unified digital ecosystem gives you:
· EDC, CTMS, RTSM, eTMF, ePRO & analytics in one place
· Study builds up to 35% faster
· >99.5% uptime with global reach
· Full interoperability with your systems
Plus, our AI automations drive:
· Smart protocol authoring
· Faster, customizable database builds
· Automated SDTM & SAS generation for cleaner submissions
Backed by:
· A team where 60%+ support full study lifecycles
· Mid-size CRO capabilities with enterprise-grade execution
· A strong security posture ISO 9001:2015 and ISO 27001:2013 (in progress)
Hybrid Delivery That Works
Hybrid delivery isn’t a trend it’s a clinical necessity.
At Oryxion, we’ve built a model that combines India-based execution with global oversight to meet the increasing demand for cost-efficiency, speed, and quality in clinical trials.
Here’s how we make it work:
Time zone advantage = faster turnaround
Cost leverage without cutting quality
Full compliance with global regulatory bodies (FDA, EMA, PMDA, CDSCO)
Secure infrastructure + ISO-aligned QMS/ISMS
Accelerating Clinical Research with Precision & Expertise!
At Oryxion, we specialize in transforming clinical trial data into actionable insights, empowering innovation, and delivering impactful outcomes.
Explore our expertise in Clinical Data Management, Statistical Programming, Biostatistics, Medical Writing, and more.
👉 Swipe through to see how we’re advancing global healthcare.
The real advantage.
At Oryxion we’ve built our delivery engine around:
⚡ Fast response times
🧠 Deep technical specialization
📊 Integrated, tech-enabled workflows
🔗 Cross-functional synergy across CDM, Stats, and Regulatory
We don’t just support studies—we build efficiencies into them.
Quality Without the Catch
“Fast and affordable” means nothing without quality.
At Oryxion, quality isn’t a checkbox — it’s a mindset. Our QA framework is embedded across all functions:
• SOP-led governance across CDM, Biostats & Programming
• Independent QA audits & dashboards
• CDISC/CDASH + 21 CFR Part 11 compliance
• Real-time deviation tracking & inspection readiness
We’re aligned with ISO 9001 & 27001 standards — because regulatory confidence starts with how we work.
Hybrid Delivery That Works
Hybrid delivery isn’t a trend it’s a clinical necessity.
At Oryxion, we’ve built a model that combines India-based execution with global oversight to meet the increasing demand for cost-efficiency, speed, and quality in clinical trials.
Here’s how we make it work:
Time zone advantage = faster turnaround
Cost leverage without cutting quality
Full compliance with global regulatory bodies (FDA, EMA, PMDA, CDSCO)
Secure infrastructure + ISO-aligned QMS/ISMS