We build quality systems for chemical and materials manufacturers. Supplier CoAs come in, get checked against spec, and go to your reviewer. Approved data turns into customer CoAs in one click. Your QC team reviews numbers instead of copying them.
Every number on a certificate traces back to the document it came from — and nothing ships on data a person hasn't approved.
PDFs and spreadsheets arrive by email, each supplier with its own layout. Someone reads each one and transcribes the values. We read them automatically and flag the ones that don't look right.
Every customer wants their own template, their own parameters, their own limits. We generate them from approved lot data — blocked automatically if the customer or product isn't qualified.
Lab results in one place, SPC charts in another, supplier data in an inbox. We put it on one lot-keyed record so SPC, audits, and customer questions all start from the same numbers.
We work with manufacturers and processors of roughly 25 to 250 people whose customers expect a certificate with every shipment — and whose QC team spends too much of the week producing them.
If your quality records live in inboxes, spreadsheets, and an SPC package nobody wants to feed by hand, we can help. We build alongside the systems you already run, so nothing gets ripped out on day one.
Industries We Serve
Customer-specific certificates generated and emailed from approved lot data in one action. Qualification checks are built in, and issued CoAs are never edited — a correction is a new version.
Scheduled pickup of supplier CoAs, production logs, and lab results. Each supplier's format is checked on arrival, so a changed layout or missing value is caught — not silently mis-read.
One queue where your quality reviewer sees each lot's data with out-of-spec flags, approves or rejects it, and closes exceptions with a comment. Every decision is attributable.
Control charts and capability on top of clean, approved data — feeding your existing SPC package or replacing it when you're ready. SPC/DOE is where we come from.
We trace how a lot's quality data actually moves today: which documents arrive, who retypes what, where specs live, and how a customer CoA gets made. You get a map of the flow and a prioritized plan.
We automate one material completely: supplier intake, review gate, and customer CoA generation, run alongside your current process until your team trusts it.
Add materials, suppliers, and customer templates on the same foundation. Then layer on SPC, history migration, and the reports your auditors and customers ask for.
We come from semiconductor process and quality engineering — SPC, DOE, specs, and supplier qualification. We know why a CoA matters before we write a line of code.
Every value is traceable to its source document, every approval to a named person, and every issued certificate is kept exactly as sent. Built for the audit, not bolted on after.
Your code, your database, your servers or your cloud. Built on standard, open tools — PostgreSQL and Python — that any competent engineer can maintain. No per-seat licensing.
We start with one material, run it in parallel with your current process, and earn the next phase. You see real certificates before any larger investment.
Start with a free 30-minute call. Walk us through how a certificate gets made today, and we'll tell you honestly what can be automated.
No pitch decks. No obligation.
Or email us directly: hello@foundrydatagroup.com