Standard operating procedures
We document each step — from collection through handover, storage, pre-thaw verification and adverse event reporting — and distribute the procedures to partner institutions. The purpose of standardization is to keep the process intact even when the people change.
Training and periodic audits
We conduct regular training and on-site inspections for contracted clinics. Recurring issues such as temperature excursions or labeling errors feed into root cause analysis and corrective and preventive action (CAPA).
Standard packages and expansion
Verified equipment specifications, procedural documents and training programs are bundled into a single standard package and transplanted to new sites. Packages validated domestically are intended to apply unchanged when entering overseas markets.
This website is intended to introduce OCELLBIO's business. OCELLBIO Inc. was incorporated in August 2026 and is currently building out its headquarters facility; the facility and equipment specifications shown are design-stage figures and will be finalized during construction and verification. Culture, quality testing and batch release of clinical-grade cells are performed by manufacturing facilities licensed under the applicable regulations, while OCELLBIO is responsible for the storage, logistics and quality documentation of cells handled in sealed condition. Specific terms of cooperation are provided on request.