Interactive Pathway Explorer
Select your project parameters to see a high-level projection of your journey with SaudiVax.
Our Embedded Expertise: A Visual Guide
We've built regulatory compliance and quality assurance into the foundation of our operations, turning potential hurdles into milestones.
Phase 1: Tech Transfer & Process Development
Our dedicated MSAT (Manufacturing, Science, and Technology) team ensures seamless onboarding. We proactively identify regulatory CQA's (Critical Quality Attributes) from day one, designing a process that is robust, scalable, and compliant by design.
Phase 2: Clinical Manufacturing
We operate under a single, fortified QMS, providing complete data integrity and batch records ready for regulatory submission (e.g., IND, CTA). Our embedded QA team oversees every step, accelerating your path to the clinic.
Phase 3: Commercial Scale & Lifecycle Support
Our facilities are built for successful PAI (Pre-Approval Inspection). We provide ongoing regulatory support for post-market activities, including variation filings and lifecycle management, ensuring a true end-to-end partnership.
Schedule Your Technical Consultation
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