Oryxion is a tech-enabled, full-spectrum Data CRO purpose-built to deliver precision clinical data services at every stage of drug development.

We provide end-to-end data services across Clinical Data Management, Statistical Programming (SDTM, ADaM, TLFs, Define.XML), Biostatistics, Medical Writing, Data Visualization, and Regulatory Affairs powered by an AI-enabled analytics engine and integrated technology platforms.

What sponsors get when they work with us:
→ A team whose collective experience spans 700+ global regulatory submissions across FDA, EMA, MHRA, CDSCO, and PMDA averaging 8+ years per team member, with 120+ years of combined SME expertise at the leadership level
→ Deep therapeutic area coverage across 20 indications from oncology and CNS to rare diseases and medical devices across all clinical trial phases (I through IV)
→ Expertise in complex trial designs: Adaptive, Basket, Umbrella, Crossover, Dose-Finding, and Equivalence
→ Delivery across 10 EDC platforms including Medidata Rave, Veeva Vault, InForm, Oracle, Medrio, and more
→ Three flexible engagement models: FSP (using your SOPs), Project/Program-based delivery, or Contract Staffing

Enterprise-grade security: MFA, site-to-client VPN, DLP, dynamic ransomware protection, and ISO 9001:2015 + ISO 27001:2013 certifications in progress. ICH-GCP, 21 CFR Part 11, and GAMP 5 compliant.

US presence in Katy, Texas. India HQ in Bengaluru, Karnataka.

📧 info@oryxion.com | 🌐 oryxion.com | 📞 +91 80 37012565

Exploring a data CRO partnership? Let's talk.

Oryxion

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