Why we started here
Quality teams in supplement manufacturing spend most of their week reading. We build agents that do that reading and hand the prepared record back to a qualified person.
The beachhead
cGMP for dietary supplements standardises the core quality workflows across the whole industry. The same master manufacturing records, the same component identity and purity testing obligations, the same quality-unit release step, at every manufacturer.
That standardisation is why an agent built for one manufacturer transfers to the next. The document layouts differ; the review obligation does not.
Contract manufacturers feel it hardest. They run hundreds of SKUs for dozens of brands, with a different specification behind each one, and the review queue is the thing standing between finished goods and a promised ship date.
Underneath the product is an Industry 5.0 view of manufacturing: human-centric, sustainable and resilient. Automation should carry the reading and the assembly, and leave judgement with the person accountable for it.
Founder
Atul Pandit
Founder
2x founder with a background in AI and computer science engineering, building automation that helps quality teams in regulated manufacturing move faster without giving up human judgement.
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