Industrial platform
Most cell preparationsare still made by hand.
A Grade B cleanroom, an open bench, and a result that rests on one operator's technique on the day.
I. The benchScroll ↓
Closed path · Source to filled vial
CellAuto closesevery step.
Closed tubing and predefined parameters, so the preparation is never opened to the room.
II. The closed pathScroll ↓
Controlled · Every tray, every run
Every batch meetsthe same conditions.
Temperature, gas and timing held to the recipe, and written to the batch record as the run proceeds.
III. The conditionsScroll ↓
CELLAUTO
Cell preparations, made like medicines
Eight years of engineering, a national research center, and systems already in production across China.
On the production floor
The value is not the machine.
It is the shift.
Moving a cell preparation out of manual laboratory work and into compliant, repeatable factory production.
Today, a cell preparation is made by hand.
In a Grade B cleanroom, built and maintained at high cost, with the result resting on one operator's technique on the day.
Every manual step is a point of variation.
Variation between operators, variation between runs, and records assembled on paper after the fact.
Closed tubing. Predefined parameters. Repeatable results.
CellAuto runs the process from source material to filled vial without an open step, and captures every parameter while it happens.
A factory standard that a regulator, an auditor and a patient can rely on.
Eight years of engineering, a national research center and systems already in production across China.
Technical patents filed across cell manufacturing automation
98invention patents granted
Developer of the National Engineering Research Center for Key Generic Technologies of the Cell Industry, and first in the world to deliver a fully automated system capable of independent MSC production.
What CellAuto delivers
Qualified cell preparations.Not just equipment.
The outcome is a qualified cell preparation, produced in one closed, compliant process from source material to filled vial.
A Grade D cleanroom is enough. One operator per batch, or continuous production, with up to 70% gain in production efficiency.
Every parameter is recorded as it runs, traceable from donor to patient and ready for audit. Proven with MSC, iPSC, NK, CIK, CAR-T and DC workflows.
The CellAuto standard
One platform,
three layers.
CellAuto is not selling machines one by one. It is not three ranges to choose between. The hardware, the specialised handling and the record keeping that together make a compliant line, delivered and validated as one.
CellAuto Series
Closed, automated cell manufacturing from source material through to final fill.
CPS040 · IDS015 · MCS015
WAVE010 · APS030 · AS015
X Lab Series
Radiopharmaceutical dispensing, lead pot circulation and waste handling, with no operator exposed to radiation.
Dispensing · Mobile · Lead Pot
Waste · Workstation
Software Series
The Cell Full Lifecycle Management Platform, with bidirectional traceability and AI-assisted process control.
R&D · Production · Quality
Resources · Compliance
Open versus closed
The moment a process is openedis the moment it can be lost.
Every manual transfer between steps exposes the preparation to the room. A closed path does not.
Manual bench
Open transfers between steps
Each open step needs a higher cleanroom grade to compensate, and the risk returns with every batch.
CellAuto platform
Closed tubing, source to filled vial
The preparation stays sealed from source material to filled vial, so a Grade D cleanroom is enough.
This is the whole argument in one picture. The cleanroom grade, the operator count and the batch-to-batch consistency all follow from whether the path is open or closed.
How we got here
Eight years building
the industrial case.
Each step moved cell preparation further out of the laboratory and closer to a production floor.
Scroll sideways →
Foundation
R&D laboratory founded in Shenzhen around a combined automation, biotechnology and information technology team.
First prototype
The world's first prototype of a fully automated intelligent cell manufacturing system, running MSC processing end to end.
Recognition
Second Prize, National Technological Invention Award.
First delivery
The world's first fully automated cell manufacturing system delivered, with independent MSC production.
Radiopharmaceuticals
China's first automated radiopharmaceutical dispensing system delivered. Recognised as a National High-Tech Enterprise.
CellAuto Matrix
Following the updated NMPA GMP guidelines, the AI-driven Matrix launched for closed, continuous, automated production.
Scale
ISO 9001 certified. CDMO platform with Fujian Maternity and Child Health Hospital, and an automated virology laboratory with the CDC.
How it works
One closed run,from source material to filled vial.
Six systems, one continuous process, and no open transfer at any point in between.
Prepare
Media and reagents enter the line through a closed tubing interface, with recipes managed automatically.
IDS015
Process
Cells are concentrated and washed in continuous flow, so viability holds while processing time drops.
CPS040
Expand
Parallel culture units and a wave bioreactor grow several batches at once, each isolated from the others.
MCS015 · WAVE010 · AS015
Fill
The finished product is filled in the same closed system it was made in, never exposed on the way.
APS030
Running underneath every phase, the Cell Full Lifecycle Management Platform records each parameter, operator action and deviation, so the whole run is traceable end to end.
One system, every scale
From a single vialto twenty-one litres.
The same closed process runs a first clinical batch and a commercial one. Nothing is re-validated on the way up.
1 mL – 21 LCPS040
Fresh, cryopreserved and expanded cells all run on the same system.
≥95%
Cell recovery through concentration and washing.
±3%
Viability held within this band across the run.
Grade D
The cleanroom grade the closed path makes possible.
Figures are drawn from CellAuto customer deployments and internal testing and may vary with process, cell type and configuration.
Inside the platform
Six systems.One qualified output.
Each one does a single job inside the closed run. Together they take a batch from source material to a filled vial without an open step.
High-Throughput Cell Processing System
≥95% recovery · Viability within ±3% · 1 mL to 21 L
Couette micro-vortex concentration and washing in continuous flow. Fresh, cryopreserved and expanded cells all run on the same system.
Intelligent Dispensing System
Grade D compatible · Multi-liquid, multi-bag
Media and reagents prepared and transferred through a closed tubing interface, so the process starts without an open step.
Matrix Culture System
Up to 10-layer factories · Automated CO₂ control
Parallel culture units, each with its own gas supply and isolation filter, and a built-in microscope that images confluency on its own.
Wave Bioreactor
Optical pH and DO · Dual-zone temperature
Suspension and microcarrier cultures expand under gentle wave motion rather than impeller shear, with two bags at independent temperatures.
Automated Positioning System
Dual-shaft motion · Fully programmable
Vessels rotated, tilted and positioned between steps under programme control, removing the handling that usually breaks a closed process open.
Fully Automated Filling System
Closed single-use path · Automated final fill
The finished product is filled in the same closed system it was made in, reaching its final container without ever being exposed.
The difference
Cell preparationstops being handmade.
What changes when a preparation moves from a laboratory bench to the CellAuto platform.
The cleanroom grade is the one that shows up on the budget. Moving a process from Grade B to Grade D changes what the facility costs to build and to run.
Deployments
Compliant production,inside the facility you already have.
The same modular architecture scales from a single hospital cleanroom to a commercial manufacturing floor.
Tertiary hospitals
Deployable in Grade D environments
Fits space-constrained facilities
Single-batch or multi-patient production
CDMO platforms
Rapid deployment, flexible scaling
Handles varied client processes
Intelligent scheduling removes bottlenecks
Manufacturing workshops
Hardware scales to mass production
Full-process software traceability
Ready for remote audit
Delivered, commissioned and co-established.
Recent projects, most recent first.
Two ways in
Start with the line,or start with your process.
Whether you are building a facility from nothing or already running a preparation, the platform meets you where you are.
01Turnkey
A compliant production line, delivered.
We deliver the capability to produce qualified cell preparations, installed, validated and running as one system.
02Tailored
Custom process development.
Already running a process? Our engineers adapt the modular systems to your workflow, cell type and scale targets.
01 / 06
Cell therapy
Cell therapies,made at scale.
One closed platform for every major cell therapy workflow, from source material to filled vial.
02 / 06
Hospitals
Hospital-grade production,on site.
CDMO platform for cell therapeutics, co-established with Fujian Maternity and Child Health Hospital, 2025.
03 / 06
CDMO
Many clients.One compliant line.
Rapid deployment and scheduling that removes production bottlenecks across multiple client processes.
04 / 06
Radiopharmaceuticals
Radiopharmaceuticals,zero exposure.
China's first automated radiopharmaceutical dispensing system, delivered 2022.
05 / 06
Quality and traceability
Every batch,traceable.
Every parameter, operator action and deviation recorded as it happens, not assembled after the fact.
06 / 06
Public health
Automated labsfor public health.
Automated virology laboratory, co-established with the Chinese Center for Disease Control, 2025.