Contact: Bring one certificate you hold. Leave with the record.

The read, in front of you

Your certificate against up to 20 named checks: every value cited to its page and line, the limits your dose allows computed and shown, and the supplier, maker and laboratory checked against 6 FDA records. You read the finding and the drafted supplier request before we say a word about it.

What you leave with

The record, exported. Your own paperwork, read the way an inspector or a patient will read it. Whether it changes anything at your bench is your call.

Prefer to look first?

Open the live demo, the real product on a seeded sample workspace where every firm and lot is fictional, with no signup. Read a certificate yourself with no account, on the same read the session uses. See how pricing works.

What the session is not

Not a sales deck and not a test of your material. We read documents. We do not test material or grade medicine.

No sales handoff

The session is a working read of your paperwork, not a pitch, and there is no handoff to a rep.

Security

Encrypted in transit. The session runs on the no-account read, which does not keep the file, its text or its name, so nothing is retained from the session unless you open a workspace.

After the session

One site, one receiving workflow, your written policy, for thirty days. You measure minutes per lot before and after. We do not quote a savings figure for you.

Twenty minutes, on your own paperwork. No slides, no handoff to a rep.

With the person who wrote the method.

Your certificate, read the way an inspector will read it.

We start where your exposure is: a certificate you already rely on. Every value is cited to the page and line it came from. Where you give the route and your largest dose, the endotoxin limit that dose allows is computed under USP <85>, K over M, with the arithmetic on screen.

Then the outside sources: whether the named maker is registered with FDA to manufacture, whether the identity matches FDA's substance registry, and whether enforcement records, warning letters or import alerts name the supplier, maker or laboratory.

The verdict heading and the one next step
The supplier request, drafted from the real gaps
What could not run, named, never counted as passed
Solvents and elements, as a share of each permitted daily exposure under ICH Q3C and ICH Q3D

The heading on a read of certificate COA-TP-3311 for pyridoxine hydrochloride lot TP-3311: your call on the manufacturer's address and telephone, printed with Halden Fine Chemicals' address in Edison, NJ; 2 checks waiting on the FDA's substance registry and the laboratory; every other check that could run verified; 7 verified, 0 failed, 4 waiting and 9 that don't apply of the 20 named checks

How certificate COA-TP-3311 was read: 17 lines and 9 values read, 2 results with a limit; checked against the 503A basis, the FDA's substance and establishment registries, openFDA enforcement records, the issuing laboratory and an independent laboratory; held to 21 U.S.C. 353a, ICH Q7 11.4, ICH Q3C and Q3D, USP <85> and <1111>, the FDA's public records, your release rules and its own figures — What the session reads, what it checks the certificate against, and the rule behind each check.

Published limits and outside sources on certificate COA-TP-3311: endotoxin, residual solvents, elemental impurities and microbial counts don't apply, each because no such result is stated on the certificate; FDA enforcement records don't apply to the sample supplier; identity in the FDA's registry is waiting, because only the name could be compared; earlier certificates don't apply, as this is the only one seen for the lot; and the laboratory's confirmation — What could not run is named, with the reason, and never counted as passed.

Four things to bring. None uploaded ahead of time.

They make the session about your operation rather than ours.

One certificate

Ideally one you already have a question about. A PDF with a text layer reads best; it is read and not kept.

The route and your dose

The route and the largest hourly dose you compound from that lot, so your limits are computed, not assumed.

The supplier's name

And the maker's, if the certificate names one. Both are looked up in FDA's records while you watch.

The person who decides

Whoever signs releases or receives deliveries. They are the one the record is built for.

Before you book.

No. Nothing is uploaded ahead of time, and in the session the certificate is read on the no-account read, which keeps no copy. One line in the form about where to start is enough.

It is a working session on your own paperwork. If the record is useful, a written scope and price follow, usually within a day. If it is not, you still leave with the record.

No patient information is needed or asked for. Bring a supplier's certificate, not a prescription. The server never receives a pharmacy's orders, patients or prescriber's words.

The Network is free for suppliers and buyers. Workspaces are priced per site, and Passports and Seals once per order. How pricing works.

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