A Partnership for the Full Lifecycle
Our commitment doesn't end at manufacturing. We are your strategic partner from initial development through long-term market supply and lifecycle management.
Phase 1: Development & Scale-Up
Collaborative process development, analytical method validation, and seamless scale-up for clinical and commercial readiness.
Phase 2: Global Market Supply
Robust, compliant cGMP manufacturing to ensure a secure and reliable supply chain for your products to markets worldwide.
Phase 3: Lifecycle Management
Ongoing support for post-approval changes, regulatory filings, and continuous process improvements to maximize your product's long-term value.
The Digital Compliance Twin
Our secure Partner Portal is more than an interface; it's your project's **verifiable single source of truth**. Explore the features below to see how we provide radical transparency and an unbreakable, audit-ready foundation for our partnerships.
Your Project's Compliance Command Center
2
Active Batches
4
Documents Pending Review
18
QA Approvals (Month)
1
Open Deviations
Your Pending Actions
Review proposed change to Batch Record MBR-08B
Project: SVX-MAB-001
Approve updated Quality Agreement v2.1
Project: SVX-VAC-003
Trusted by leaders in research, healthcare, and biopharma
Ways to Partner With Us
We offer flexible partnership models designed to meet your strategic objectives.
CDMO Services
Leverage our state-of-the-art facilities and expert teams for process development, clinical supply, and commercial-scale biomanufacturing.
Inquire about CDMO →Strategic Alliances
Collaborate on the co-development of novel biologics and vaccines, from late-stage research through to regulatory approval and commercialization.
Propose an Alliance →Technology & Innovation
Engage with us on technology in-licensing or out-licensing opportunities to accelerate the development of next-generation therapies.
Discuss Technology →Already a Partner?
Access your secure project dashboard for real-time updates, data exchange, and collaboration tools.