AI changed what can be imagined.
Invitris changes what can be delivered.
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AI can now design drugs faster than today's manufacturing infrastructure can produce them. We strive to mass-manufacture individualized drugs.
AI has reached a stage where modeling proteins (antibodies, phages, vaccines, etc.) has become democratized. Designing fully de-novo proteins for individual targets is now possible.
The infrastructure was designed for one drug at scale, not millions of variants at single-patient economics. This creates the new bottleneck: mass manufacturing. One-size-fits-all drugs are not the basis of a future where patients are treated algorithmically.
From sequence to drug substance in four to eight hours, built for the economics of individual medicine.
One machine. Any protein/drug. In hours.
Under GMP. Aseptic. End-to-end. For a wide range of protein classes.
Single-step process. Autonomous processing.
Built for the economics of individual medicine, not one-size-fits-all.
From digital sequence to physical molecule.
Gross margin at $1–2k COGS vs. $5–10k traditional.
More output than the leading technology.
Less endotoxin — cost-effective purification.
Microbial evolution leads to the largest health-economic problem of our time: antimicrobial resistance (AMR). Tailoring antimicrobials such as bacteriophages is key to minimise resistance and maximise efficacy.
Protein-based therapies, including antibodies, multispecifics, peptides, enzymes, and cytotoxic proteins. Perfectly designed to integrate into a therapeutic process enabled by AI modeling.
We're building Invitris Pods — autonomous biomanufacturing machines for decentralised, on-demand production. No supply chain dependency. Countries produce what they need, where they need it.
From your design, at clinical pace.
Computational design coupled to high-throughput wet-lab validation.
The design-test loop closes in days, not quarters.
One platform, from first screen to GMP-relevant volumes.
"Invitris is leading the way on advancing the pace of AI-guided design for the production of therapeutic products. Their autonomous GMP manufacturing capabilities set them apart."
Programmable reactions that turn DNA directly into functional proteins,
antibodies, and phages — no fermentation, no host cells.
Microfluidic screening at a throughput that was simply not
possible with conventional expression systems.
Computational design coupled to high-throughput wet-lab validation
close the loop in days, not quarters.
Seamless scale-up from screening droplets to GMP-relevant
production volumes on a single platform.
July 30, 2026

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November 1, 2022