The Evidence Operating System for Compounded Medicine

Know what you received.Prove what you released.

Raw ingredient to finished medicine.
Every hand on the record.

Every ingredient needs valid paperwork. The law never says how to check it.

Paperwork is the only thing that travels with the medicine. Three public records say the same thing from three sides.

United States Code21 U.S.C. §353a(b)(1)(A)(iii)

… accompanied by valid certificates of analysis for each bulk drug substance …
The law asks for a valid certificate with every bulk substance.

FDA warning letterMay 1, 2026

… identified your firm, “…,” as the manufacturer of API rather than (b)(4), the firm from which you purchased …
A certificate can name the seller and leave the maker off.

NABPJuly 29, 2026

… the absence of supply-chain traceability tools for compounded products, and the difficulty of verifying the bulk substances from which compounded medications are made …
The boards of pharmacy name the missing tool outright.

Quoted and attributed. No affiliation or endorsement implied.

Today, the record is in pieces. Filed, logged, never checked.

Your log proves a certificate arrived. It cannot show who checked it, against what, or what they found.

A shared drive of certificates, each marked on file with no reviewer, beside a receiving log with an empty Checked by column

That tool now exists.

Supply-chain traceability for compounded medicine.

One lot, from certificate to patient. One record the whole way.

Verify

Every certificate, and everything behind it. Held to the statute, FDA's records and the limits for your dose.

Twenty checks on each certificate, with limits computed for your dose. The same review reaches the supplier, the maker, the laboratory that signed it, the order it fills and the file itself. Every finding about the certificate opens on its page and line.

  • Certificates20 checks, limits for your dose
  • Suppliers37 items, each with its source
  • ManufacturersFDA registered to manufacture
  • LaboratoriesAccredited scope, asked to confirm
  • OrdersEssentially-a-copy evidence, per order
  • The file itself17 integrity signals
  • PotencyEach lot's factor, from its certificate
  • Sterile recordsRead against USP <797>

Everything behind lot BM-5520: the certificate not verified and the maker not named, the limit, supplier, lab, file and order checked
Lot BM-5520 arrives from Brookmere API Supply. Its certificate names the seller, not the maker, so the lot is held.

Built from the product, on a sample workspace. Every firm, lot, person and number in it is fictional.

The Review

How a certificate is read and checked

It arrives and is kept as it came

Emailed, uploaded or sent by the supplier on one free link. The original is kept exactly as received, and fingerprinted the moment it lands.

Every line is read and numbered

Each value keeps its page and line, so a finding opens on the line it came from.

Twenty checks, with the arithmetic shown

The certificate's own figures and dates, the 503A routes and FDA's 503A lists, the ICH and USP limits computed for your dose, FDA's registries, and every certificate seen before for the lot. Each check names the standard it applies.

Held for a named person

What does not hold up says what was found, what is required and how to clear it. Nothing is released until a named person decides, and the reason is kept.

Open the full page

Supplier files

How a supplier file is kept

Every credential says how it was established

Matched at the source by Veritura, confirmed by a named person, on file but not verified, or missing. A negative result is a result, and a lookup that did not run says so.

Missing documents, requested in a draft you send

When a quality agreement or a corrected certificate is owed, the request is drafted for you and waits for a person to send it.

The Network, free

Publish and find suppliers, follow a supplier. Free for pharmacies, clinics and patients.

Open the full page

Release and Passports

How a lot is released and proved

Released by a named person

Nothing leaves a lot until a named person reviews it and signs. Their name, the decision and the reason stay on the record.

Proof travels with the medicine

Every cleared order carries a serialized Passport. Scan the label to see what was checked, against what, and who decided. No account. No app.

Hundreds of Passports from one order

A cleared order can issue a unit Passport and a serialized Seal for each of up to 500 units in one run, charged once for the order, with the full delivery trail kept on the order.

Open the full page

Trace and recall

How the record follows the medicine

Back up the chain

Each order points to its lot, the certificate read for it, the supplier packet behind it and the person who released it.

Hand to hand

One code on the box, one Seal per vial. The clinic scans to receive, one scan at the chair writes the administration line, and the patient sees the chain.

A recall that reaches every desk on Veritura holding the lot

Declare it once. Every desk holding the lot sees the recalled vials named, and you see which clinics have opened the notice.

Open the full page

Rehearsed before the inspector arrives. Two agents do the legwork. People decide.

By default Vera drafts and a person sends; she never makes a first contact or a release on her own. Cato rehearses the inspection before an inspector arrives.

Vera, overnight: a certificate for lot BM-5520 arrives, is read line by line and checked; the original manufacturer is not named, so the lot is held; Vera drafts the request to the supplier, a person sends it, the corrected certificate clears the lot, and Vera lines up the 5 Passports, one per order, that one signature issues. Cato, in a mock inspection, asks the 46 things an inspector commonly asks a pharmacy for, answers each from a record or counts it as open, and a person files the rehearsal: 22 confirmed by a person, 2 checked by Veritura, 3 shown in person, 3 still to collect, 6 missing; 10 do not apply there.

Vera drafts. A person decides.

Requests, findings and next steps are drafted for you and wait for a person to send them.

Meet Vera
Cato counts what an inspector will ask for.

Each record is ready, in review or missing, in the order inspectors usually ask, with no score.

Meet Cato

Open a sample lot. No sign-up, nothing to install.

Today in the sample workspace: lots to review, one held for a person, four ready to release, and the dates coming up
Open the live demo

A read-only workspace seeded with sample lots. Every check, citation and hold, as the product shows them.

Open the live demo
A sample Passport for cyanocobalamin 1,000 mcg/mL: paperwork reviewed, assay inside its printed limits, no recall notices
Scan a sample Passport

Point your phone’s camera at the code. It opens what a patient sees: what was checked, against what, and who decided.

Open the sample Passport

Questions, answered plainly. Know what the record proves before you rely on it.

Veritura is deliberately narrow. Here is what it does, and what it will not claim. Read the methodology

What does Veritura actually verify?

The documentation, against standards outside it: the 503A routes and FDA's 503A lists, the ICH and USP limits computed for your dose, FDA's registries and enforcement records, the certificate's own arithmetic and dates, and every certificate seen before for the lot. Every finding about the certificate cites its page and line. We do not test, grade, or endorse the medicine itself.

Does Vera make release decisions?

No. Vera reads the packet, drafts a cited finding, and prepares the next action. A named person confirms every material decision, and their signature, reason, and policy version stay on the record.

What happens when the evidence is incomplete?

The gap stays visible. Veritura records what could not be verified and routes the next action, so missing evidence never quietly becomes a pass.

Where does the patient’s contact live?

Not in the clinic’s or the pharmacy’s record. The clinic’s administration line carries the unit, the lot, the date and the clinic’s own visit reference. A patient who scans the vial can save it to their own space with an email they type themselves; that email lives in the patient’s account, and Veritura never joins it to the clinic’s record.

Who pays, and what is free?

Patients and clinics pay nothing: reading the record from the vial, the receiving desk, the recall net and the patient page are free at any number of sites. The operation that reads the paperwork pays: a pharmacy or 503B on Essentials, Workspace or Operations, a platform on Operations or a quoted scope. The Network is free for everyone.

Who can see the proof?

Anyone you give the code to. The public page shows what was checked, against what, and who decided, along with the boundary of what that evidence supports.

Checked against the public record, every time.

Dated503A listsFDA's lists: whether the substance may be compounded at all
Every readFDA registriesThe maker is registered to manufacture, not only to repack. The substance's identity, both figures shown on a conflict
Every readUSPWhether a monograph exists, one of 503A's three routes
Every read, then hourlyopenFDAEnforcement records for the supplier, the maker and the laboratory, with FDA warning letters and import alerts searched apart at read
With your doseUSP <85>With ICH Q3C and Q3D: the limits your route and dose allow, computed
Live lookupNPPESThe prescriber's and the pharmacy's NPI

The codified 503A lists are re-read every 24 hours; FDA's Category 1 and 2 lists are a dated capture, May 14, 2026. Each lookup keeps its source and the date it ran.