Your certificate against 20 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.
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. Use a public tool with no account. See how pricing works.
Not a sales deck and not a test of your material. We read documents. We do not test material or grade medicine.
The session is a working read of your paperwork, not a pitch, and there is no handoff to a rep.
Encrypted in transit, access-scoped to your workspace, nothing retained from the session unless you open a workspace.
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 We do not quote a savings figure for you.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.
In the session
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
Before the session
Four things to bring. None uploaded ahead of time.
They make the session about your operation rather than ours.
Ideally one you already have a question about. A PDF with a text layer reads best; it stays on your screen.
The route and the largest hourly dose you compound from that lot, so your limits are computed, not assumed.
And the maker's, if the certificate names one. Both are looked up in FDA's records while you watch.
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 the certificate stays on your screen. 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.
Rather write? The form above reaches the same inbox.