Fillix
Fill and dose control for aseptic lines.
The autonomous operations layer for sterile pharmaceutical fill-finish: aseptic filling, seal and CCI, lyophilisation, AI visual inspection, contamination control.
Sterira closes the loop on sterile fill-finish: aseptic filling and dosing, seal and container-closure-integrity, lyophilisation optimisation, AI visual inspection, contamination control and robotic handling.
Each line deployment produces labelled inspection and batch traces that train the next model, tightening the loop from fill to final inspection.
| Detail | Value |
|---|---|
| Stage | Seed |
| Category | Physical AI |
| Year | 2026 |
| Website | sterira.com |
| Headquarters | Not disclosed |
| Raised | $1.5M |
| Investor | 10xC |
| Model | Per-line software subscription with validation support, entered through a pilot on one inspection step. |
| Measured by | False-call rate, inspection throughput, batch release time, lines expanded per customer. |
Every deployment on sterira.com writes labelled traces back into the model, so the system generalises across plants, alloys, grades and geometries.
Fill and dose control for aseptic lines.
AI visual inspection for particles, cosmetic defects and CCI.
Lyophilisation cycle optimisation.
Aseptic and contamination-control intelligence.
Robotic handling in the isolator and on the line.
Aseptic-line digital twin for validation and what-if.
Sterile fill-finish is the most regulated bottleneck in pharma: lines that can take months to qualify, inspection that still leans on human eyes, and a skills base concentrated in a few hands.
Sterira sells the audit trail as the product. The buyer is a CDMO or pharma manufacturer paying in hard currency; the wedge is one inspection step, and validation evidence is the flywheel that pulls each next module onto the line.
David owns the pharma relationships, qualification strategy and the commercial model.
Grace owns the vision models, the edge runtime and the GMP-grade audit architecture.
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