SaudiVax
Capabilities

Sovereign Biomanufacturing at Scale

End-to-end CDMO infrastructure engineered for national healthcare self-sufficiency. 200,000L bioreactor capacity across ISO 5 cleanrooms, fully aligned with SFDA and FDA standards.

Digital Twin

Jeddah Biomanufacturing Facility

Interactive facility overview. Select a system to view technical specifications.

A — Upstream B — Downstream C — Fill-Finish D — QC Analytics 22.4°C pH 7.2 BR-01 · 20kL Fed-Batch 36.8°C DO 42% BR-02 · 20kL Perfusion Δp 0.3 bar CHR-01 · AKTA IEX+SEC UF/DF-01 TFF 30m² ISO 5 ΔP +15Pa FF-01 Isolator −50°C <1% RH LYO-01..04 ENV:OK 24/7 QC-01 · HPLC+MS USP/EP EMS-01 VIABLE+NVC
System Specifications

Select a zone on the facility map or choose below.

Interactive floor plan — Jeddah Biomanufacturing Facility. Select a zone to view specifications.

CDMO Services

End-to-End Manufacturing Solutions

From strategic market entry advisory to full-scale commercial manufacturing, our integrated platform eliminates hand-off friction across the product lifecycle.

Scale Biomanufacturing

Leverage our 200,000L capacity for process development, clinical supply, and commercial-scale production of biologics and vaccines.

  • End-to-end process development
  • Single-use bioreactor technology
  • cGMP fill-finish services

Accelerate Clinical Development

Our Innovation Hub advances promising candidates through late-stage R&D, process validation, and regulatory milestones.

  • Late-stage asset co-development
  • Analytical method development
  • Tech transfer & scale-up support

De-Risk Market Entry

Our Advisory platform provides unparalleled local insight, regulatory navigation, and strategic partnership mapping for MENA market entry.

  • Regulatory affairs strategy
  • Market access & health economics
  • Stakeholder & partner mapping

Digital Quality Infrastructure

Our inspection-ready Quality Management System is the cryptographic foundation of the Jeddah biomanufacturing hub.

AUDIT-READY

Unified Data Integrity

A single, embedded QMS ensures cryptographic data integrity and a complete audit trail from day one.

PROACTIVE

Anticipatory Compliance

Proactive, digital quality assurance anticipates regulatory needs, accelerating tech-transfer timelines.

VERIFIED

Market Certainty

Always inspection-ready for SFDA, FDA, and EMA auditors — providing absolute market certainty.

Integration

The Integrated Value Chain

You don't just get a vendor — you get an end-to-end sovereign partner. Engage us at any stage for a compliant, accelerated pathway to clinical and commercial scale.

01

Advisory

Market strategy, regulatory affairs, and stakeholder mapping

02

Innovation

R&D, clinical acceleration, and process development

03

Manufacturing

At-scale production, fill-finish, and global supply

Ready to Manufacture at Scale?

Explore how our sovereign biomanufacturing infrastructure can accelerate your pipeline from development to commercial supply.