Systems

Process systems for lipid nanoparticle formulation.

SC Biosystems is developing high-pressure mixing and fluid-control equipment intended to connect early formulation work with reproducible scale-up and production.

A common process environment

Development and manufacturing should not begin as separate systems.

Our systems programme is organised around the process variables that must remain controlled as material use, throughput, and downstream requirements change.

01

Development

Controlled material use, flexible process definition, and rapid iteration for early formulation work.

02

Scale-up

Common process variables and control logic for understanding how operating conditions translate across throughput.

03

Manufacturing

Integrated pumping, pressure management, conditioning, automation, and process records for larger-scale operation.

Formulation workflow

The mixer is one part of the process.

Defined inlet conditions, high-pressure mixing, immediate conditioning, and analytical feedback all contribute to the formulation that emerges. Equipment development therefore has to consider the complete operating environment.

Software-defined process control

Instrumentation and software designed as one system.

SC Biosystems builds on a background in engineering software, automation, and industrial control. That experience shapes how process conditions are defined, monitored, recorded, and reproduced.

01

Recipe control

Defined process sequences and operating parameters.

02

Flow and pressure

Continuous visibility of critical fluid conditions.

03

Process data

Structured records connecting operation to formulation outcomes.

04

Automation

Coordinated pumps, valves, mixing, and downstream actions.

05

Repeatability

Consistent execution across development cycles.

06

System diagnostics

Clear operating state and practical fault identification.

Development work

See these process technologies applied across lipid nanoparticle formulation and automated oligonucleotide synthesis.

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