Organoid chips
We are a one-stop CDMO for organoid-on-a-chip and organ-on-a-chip programs: chip design and engineering, PDMS rapid prototyping, thermoplastic injection molding for scale-up, glass and silicon MEMS processing, surface functionalization, bonding, assembly and QC — all delivered inside an ISO 13485 quality system.
Six capability blocks covering the full chip lifecycle
Design-for-manufacturing review of your architecture: channel geometry vs. shear budget, membrane pore selection, dead-volume optimization, and material selection (PDMS, COC/COP, PMMA, glass, silicon) matched to your assay chemistry.
Fast iteration on soft lithography: master fabrication, PDMS replica molding, plasma bonding, and interchangeable layer stacks. The fastest route from a literature design to a working device in your lab.
Transfer your prototype into a thermoplastic cartridge: tool design, ISO 7 cleanroom injection molding of COC/COP/PMMA/PS, thermal and solvent bonding, and validated process windows for volume production.
High-rigidity, optically superior substrates for advanced assays: etched silicon and glass microstructures, anodic bonding, and hybrid glass-plastic assemblies with sub-micron feature fidelity.
Assay-critical surface chemistry: ECM coatings (Matrigel, collagen I/IV, fibronectin, laminin), plasma and chemical grafting for wettability control, bubble-free priming treatments, and drug-adsorption mitigation strategies.
Turnkey cartridge build-outs: membrane integration, reagent lyophilization, pump and valve integration, SBS-format plates compatible with standard handlers, plus dimensional, leak and burst testing on every lot.
Concept to clinical-grade supply in six gated stages
Technical deep-dive on your assay, organoid model and throughput target. NDA within 48 hours.
Week 0–1Architecture review, material and process selection, CAD/GDS readiness, fixed-fee quote per stage.
Week 1–3PDMS or machined thermoplastic iterations with defined test criteria: flow, bonding, cell viability.
Week 3–8Verification builds against your acceptance protocol; dimensional, leak, burst and surface QC reports.
Week 8–14Tooling, cleanroom molding process lock, first article inspection, assembly line qualification.
Week 14–24ISO 13485-controlled release, lot traceability, capacity ramp to millions of cartridges per year.
Ongoing
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