Dashboard
Free plan

API

Every key this workspace holds, in one place: test keys, live keys, the metered passport key, and your webhooks.

Secrets shown onceSigned webhooksTest before live
Which key is which
Metered passport key · vtr_live_…

Does one job: issue an Evidence Passport per order at $3 each, first one free. Included with Evidence Passport production, so Clinic plans and up hold one, as does any account that activated with a card. Managed just below.

Full API keys · vk_test_ / vk_live_…

Nine /v1 endpoints, named one by one in the Developers card below: document check, passports, seal batches and their label formats, ClearGate decisions, the network directory, a single network source, network routing, and eligibility. Both modes belong to the Facility plan ($399/mo). A test key needs the same entitlement as a live one, so it is not a way in without the plan; what it does not do is cost anything to run or touch production records.

Connect your system orders arrive on their own, two ways, pick either or both
The daily drop

Point your pharmacy system's scheduled shipment export at a folder and run the watcher: each file posts itself, passports issue and release under your policy, and you get a digest of anything that needs you. The export is parsed in memory; only order, lot, and email are kept, the raw file is never stored.

Or POST the file yourself: POST /api/passport-drop with {"csv":"…"} and your metered key. Setup instructions are inside the script.

The order webhook

Real time, per order: any platform that can send a webhook when an order ships (a Zapier or Make step, or your fulfillment system's own webhook) POSTs to your private URL and the passport exists the same second. Field names are matched tolerantly, so most payloads work unchanged.

Recipe: in Zapier or Make, trigger on your platform's "order shipped", add a Webhooks POST step to your URL, map order number and lot. Rotating the URL invalidates the old one.

Developers · API & webhooks Facility plan ($399/mo)

Issue Evidence Passports on order straight from your fulfillment or pharmacy system: create a key, then call POST /v1/passports with an order and a cleared lot. API keys (test and live) are part of the Facility plan; live keys issue real production passports and need a production workspace.

Embed the Trust & Traceability Network in your own ordering flow: GET /v1/network/directory (grade-ranked verified sources), GET /v1/network/source?source=<id> (a source's portable grade + trust signals), and POST /v1/network/route (ship-to-state Allow / Review / Hold). Read-only, documented status only. For platforms and GPOs that want the network inside their own product.

Print Veritura Seals from your own system: POST /v1/seal-batches mints up to 500 serialized vial seals for a lot (optionally bound 1:1 to your order numbers), and GET /v1/seal-batches/<id>/labels?format=avery|thermal|zpl returns the labels: Avery 5160 PDF, thermal-roll PDF, or raw ZPL your networked label printer can be fed directly (port 9100 or a raw print queue, no driver in between). Same plan entitlement as sealing from the dashboard.

# 1 · mint order-bound seals for a lot
curl -s https://www.veritura.co/v1/seal-batches \
  -H "Authorization: Bearer vk_live_..." -H "Content-Type: application/json" \
  -d '{"lot_id":"lot_...","count":3,"order_refs":["RX-88101","RX-88102","PO-7231"]}'
# response: { "batch_id": "sb_...", "serials": [...], "labels": { "zpl": "/v1/seal-batches/sb_.../labels?format=zpl", ... } }

# 2 · feed the labels straight to a networked Zebra-class printer (no driver)
curl -s "https://www.veritura.co/v1/seal-batches/sb_.../labels?format=zpl" \
  -H "Authorization: Bearer vk_live_..." | nc printer.local 9100
# or, on a CUPS raw queue:  ... | lp -d zebra -o raw

These vk_ keys are separate from the metered Evidence Passport key on the Passports page: vk_ keys power full /v1 integrations (passports, seals, ClearGate, the network), while the metered key does one job, issuing passports at $3 per order.

What /v1 contains every route this server answers, and what each one needs
The server is the authority. Where this table and a live response disagree, the response is right and this table is stale. Webhooks are not a /v1 route: you register a delivery URL below and Veritura POSTs to you, signed. Every route answers 401 without a valid vk_ key, and the key mode decides the environment: a test key writes to the sandbox, a live key to production.
RouteWhat it doesBeyond a valid key
POST /v1/checkReads one document and returns its extracted fields and findingsRate limited per key, plus a concurrency gate that answers 429 with Retry-After
POST /v1/passportsIssues an Evidence Passport from a cleared lot on your ledgerThe lot must be yours and cleared. Metered at the passport rate
POST /v1/seal-batchesMints up to 500 serialized vial seals for a lot, optionally order-boundSame seal allowance as the dashboard button; the API cannot out-mint the plan
GET /v1/seal-batches/<id>/labelsReturns those labels as avery, thermal or zplThe batch must belong to the key’s workspace, or 404
POST /v1/cleargateHolds a lot against your own documentation policy and signs the decisionWrites a signed, logged decision. Conformance to your policy, never an approval
POST /v1/eligibilitySubstance plus facility type, returned as your policy’s Allow, Review or HoldWrites a signed, logged determination. Runs live FDA shortage and NDC checks
GET /v1/network/directoryThe published verified-source list, with the grade schema in the same responseRead only. The response states what the grade counts and what it does not
GET /v1/network/sourceOne published source by its share id, with its documentation gradeRead only. Unpublished or unknown ids answer 404
POST /v1/network/routeShip-to-state gate for a published source: Allow, Review or HoldRead only against documented distribution status
API keys
Both buttons need the Facility plan ($399/mo). Test and live keys are gated identically, so pressing New test key without that plan answers The /v1 API is part of the Facility plan and creates nothing. A test key carries no per-call charge once you hold the plan.
Rotate a key by creating a new one and revoking the old. A secret is shown once, on creation.
Webhooks

In plain terms: we POST to your URL the moment a passport issues or a recall hits one of your lots, so your own system knows without anyone checking a dashboard.

Events sent: passport.issued · lot.recall_hit · supplier.alert. Each delivery is signed (HMAC-SHA256) in the X-Veritura-Signature header.

Your workspace

Your supplier qualification files, continuously verified. Screen an order or run a check to start.

Your supplier qualification files, continuously verified against live FDA enforcement and recall records: screen orders before anything arrives, review COAs per lot, and every signal reaches the file automatically.

Supplier documentation on file
FDA registration · Accreditation · COA per lot
Documentation posture, not an approval
Evidence operation

Your evidence chain starts with one check.

Every document you run becomes a logged, defensible record: read off the certificate, screened against live FDA-source data and cross-vendor forensics, and resolved to a posture you can show a board or an inspector. Not a one-off check, a system of record for your supply.

Run your first check 3 free checks, no card
Every check resolves to one posture
Clearreading complete, no conflicts
Reviewa flag or gap to clear first
Holdblocked until it is resolved
Live regulatory signal is loading…
Check activityDocuments run across your suppliers, last 12 weeks

Run a check

Drop any document and it becomes a logged, dated record with a clear posture, so a supplier's paperwork never has to be taken on faith.

Live FDA sources when a source is namedCross-vendor forensicsPaperwork verified, never the product
Run a check

Drop any document and we’ll route it, or pick a specific check.

Facility

Drop a document to start a check

COA, supplier packet page, license, or registration. The engine reads it and classifies the document type as part of the check.

PDFPNGJPGWEBP
or choose a specific check

A single COA, checked against the anonymized cross-vendor index plus signature & document forensics, then logged as a lot with a clear posture you can act on.

Drop a COA here, or click to choose

Checked against the cross-vendor index, signature & document forensics, and live FDA-source records.

PDFPNGJPGWEBP
PDF
file.pdf
Ready, runs your real engine
Document forensics Live FDA-source Cross-vendor reuse Review-ready signals

Mark what your supplier packet includes, against what a facility needs to onboard a supplier (manufacturer vs distributor identity, registration, quality agreement, and a consistent document trail). This is a self-assessment of completeness; route the packet for the full reviewed source-chain memo, memo-safe only after human review.

Required to onboard · check what you have provided

Check a supplier or product against FDA source records, registration, enforcement, recalls, and unregistered-source signals. Signals only, not an FDA approval, clearance, or registration confirmation.

Routing

Every packet you route through Veritura, with status, memo delivery, billable attribution, and your commercial terms in one place.

Live packet statusMemo delivery on the recordBillables tracked from delivered work

Suppliers

One living qualification file per supplier, so nobody re-vets from scratch at reorder time.

Re-verified vs FDA recordsReadiness: ready · gaps · holdEvidence map across your base
Bring your supply base paste it once; every supplier gets a living file, every substance goes under daily FDA watch
Records land instantly; live FDA source checks stream into each file over the next minutes. Up to 50 suppliers and 100 substances per import.
Qualify a supplier documentation readiness, not an approval

Run a supplier's full packet: attach the COA, SDS, certificate of conformance, GMP certificate, BSE/TSE statement and more. Each document is classified by type and read, with a completeness rollup. Documentation diligence only.

Evidence map suppliers · documents · lots · orders, as you build them
Suppliers

Track your whole supplier base

Qualify suppliers and keep them continuously verified and monitored. Included on the Clinic plan.

Screen an order

Gate every order against your own policy before money moves, so a bad source is caught before it ships, not after.

4 rails · one signed verdictLive FDA lists + NPPESReplayable decisionsYour policy, never an approval
Order screening console Policy loading…
Supplier ClearGatedocumentation vs your policy
Substance eligibilitylive FDA lists
Prescriber registryNPPES, live
Qualification fileyour supplier record
All four rails fire; the worst rail governs. One signed verdict, a decision against your policy, never an approval.
Example output
MEETS YOUR POLICYComposite verdict, signedoin_9f27…ae1 · sha256 chain
Supplier documentationmeets policy
Substance eligibilityFDA lists · clear
Prescriber registryNPPES matched
Qualification filecurrent
MEETS YOUR POLICYNEEDS REVIEWDOES NOT MEETthe worst rail governs · every decision names its reason
Run a screen and the four rail verdicts, live FDA feed stamps, and the signed decision land here.
Decision log signed, tamper-evident, replayable
Your ClearGate policy you set the bar; a decision means "meets your policy"

Gate every order against your policy

ClearGate turns your supplier files into an Allow / Review / Hold decision at order time, with a signed, replayable record. Included on the Clinic plan.

Recall

Everything that left the building, by lot. Most recalls reach you from the supplier days before they reach an FDA list, so this does not wait for the feed: pick the lot, say what happened, and every patient we can reach is told while you work the call list for the ones only you can reach.

Supplier-first, no feed requiredPassports, seals and slips per lotPatients notified in one clickDocumentation diligence only

Lots

Your system of record: every check becomes a lot that accretes evidence toward cleared, and a cleared lot is what portable proof issues from.

Evidence accretes per lotLive recall watchPassport-ready when clearedDocumentation diligence only
Board-Ready inspection packet

One click pulls your lots, suppliers, issued passports, and any FDA enforcement/recall exposure into one inspector-ready PDF, organized for a board or FDA records request. Documentation diligence only, not a determination of compliance.

Generate packet (PDF)
Lot ledger
Suppliers on file

Each supplier you check builds into a living dossier here: its lots, its diligence, and what is cleared versus flagged. Documentation diligence only.

Receiving Gate

The intake gate for each shipment: match the label to the paperwork, read the micro evidence, and set the lot state before anything moves downstream.

Label vs COA matchSterility & endotoxin read as evidenceSets the lot stateDocumentation release support only
Log a compounded preparation (MFR / compounding record)

Paste the record and it reads what it can; anything you type below wins. The preparation becomes a lot that clears on its class’s document set: the record itself, its beyond-use date, each ingredient traced to a verified lot (or, for a manufactured source drug, its FDA NDC directory listing), and sterility evidence when the preparation is sterile.

Sterile? Made from?
Ingredients
Receiving records
0
Release ready
0
Quarantine
0
Hard hold
0
Snap the delivery paperwork the fast path · one photo, no typing

Photograph the COA or packing slip that came in the box. The document engine reads the supplier, product, and lot, runs the same receiving gate as the form below, and hands back the shelf answer: RELEASE or QUARANTINE, with a printable green or red shelf tag for the tote.

Documentation receiving gate only. This does not determine product quality, safety, efficacy, compliance, or FDA approval.
Receive a lot identity, micro evidence, source screen
Shipment identity
Evidence & screens
Optional: the engine reads the container label and confirms product, strength, and lot itself, upgrading this from your word to a machine read.
Optional: the engine reads the report's own stated outcome (clean transit or excursion), quoted verbatim on the gate.
Run it to earn a verified Clear; a hand-picked Clear records as claimed-unverified.
Documentation receiving gate only. This does not determine product quality, safety, efficacy, compliance, or FDA approval.
Decision console gate register + supplier request
Ready for the next shipment

Run the gate to get a lot state, gate-by-gate evidence result, next actions, and a supplier request draft.

Receiving log
0 selected
DSCSA supply-chain record chain-of-custody for the manufactured drugs you buy, no COA needed

Store the Transaction Information & Statement (TI/TS) your wholesaler already sends with each manufactured-drug purchase, keep it for the DSCSA 6-year retention window, and check the trading partner against public FDA data. This desk is for the finished manufactured products you purchase. Documentation recordkeeping only.

Why your own preparations are not in this log. The DSCSA definition of “product” (FD&C Act section 581(13)(B)) excludes a drug lawfully compounded in compliance with section 503A or 503B, so the section 582 product tracing requirements, the transaction information, transaction history and transaction statement that this log stores, do not attach to it. That exclusion turns on the specific preparation and transaction meeting those conditions. It is not a blanket exemption for anything described as compounded, and Veritura does not determine whether any preparation meets them. Other section 582 duties, including authorized trading partner status and suspect or illegitimate product handling, are assessed on their own terms and are not answered by this log. Source: FDA, DSCSA Product Tracing Requirements FAQ · read 2026-07-30 · next review 2027-01-30. Not legal advice; confirm scope with your own counsel.

Unlock Receiving Gate

Convert each shipment into a documented gate decision before it reaches your lot ledger, memo file, audit binder, or Evidence Passport workflow. Included on paid workspaces.

Your order channel

Your own branded ordering front door, so buyers see the evidence behind every preparation instead of chasing you by phone and fax.

Invite-only buyersEvidence chips live from your lotsPassport on fulfillmentPrescriptions travel as they do today

Place an order

Order from the channels you were invited to, with the verification evidence in view before you commit.

Evidence before you orderStatus thread afterBusiness details only, never patient info

Formulary

Each substance you enrol here is held as one living record and re-checked against the FDA lists daily, so a list change never reaches you weeks late through a newsletter. Nothing is watched until you add it.

Daily FDA list check per enrolled substanceChange-day alertsLots + signed decisions attached503B worksheet export
Substance files current FDA list position + your policy's decision, never legal advice

No formulary items are being monitored. Nothing on this page is checked against the FDA lists until you enrol a substance below. Once one is enrolled, its file carries the list it was checked against and the date it was read, on the file itself.

503B product report worksheet a draft prepared from your records, never a filing

Outsourcing facilities report every compounded product to FDA twice a year. This worksheet pre-fills the drug-identity and source columns from the lots you logged in the reporting window, and marks every FDA-required production column for manual entry. Your facility remains responsible for its SPL submission via FDA's electronic system.

Daily FDA list checks on the substances you enrol

Each substance you add becomes a living record with its FDA list position, your lots, your decisions, and a change alert the day FDA moves. Nothing is monitored until you enrol it. Included on the Clinic plan.

Launch a service line

Name a new therapy line and its launch record computes live from what your workspace already knows, so "are we ready to offer this?" has a documented answer.

6 launch elements, liveStamped attestationsFormulary from day oneOne dossier PDF

Launch a therapy line with the record already built

Signed eligibility decisions, formulary verification from day one, cleared-lot evidence, supplier qualification, the ordering rail, and your own stamped attestations, exported as one launch dossier.

Capability required
Supplier tracking and monitoring (supplierTracking). The same capability opens Suppliers, Formulary and Sourcing, so unlocking it here unlocks those too.
Feature tier
Clinic, $99/mo. A feature tier is a commercial level, not a facility type: your workspace type is set in Settings and upgrading does not change it.
Data you need first
None. Every element computes from records you already hold, and an element with nothing behind it says so rather than blocking the dossier.
Where upgrading returns you
Checkout returns to your workspace, not to this screen. This screen is Formulary → Launch a service line in the sidebar: open it again and the launch record is here. Nothing is entered on this screen while it is locked, so nothing is lost on the way.

Sourcing

Type a substance and see which 503B facilities reported compounding it to FDA, and where it stands on the live shortage list, so a shortage becomes a documented sourcing conversation instead of a scramble.

Live FDA shortage board503B product reports, by reporting windowFacility standing per resultSigned sourcing memos
Facilities that reported compounding this FDA-published facts, not recommendations

Live FDA shortage status plus every 503B facility that reported compounding the substance to FDA.

Reported compounding is not current availability. A 503B product report is a retrospective filing: it says what a facility told FDA it compounded during a past reporting window, and every row here carries that window and the date the data was read. It does not establish that the facility produces the preparation now, holds stock, has capacity, or will sell to you. “Can supply” needs a dated attestation from the facility itself, and no result on this page carries one.
Where these results come from

Every result is built from FDA's own published data: the drug shortage list, the biannual 503B product reports, and the registered outsourcing facility list, joined with the network's documented coverage. What a facility reported compounding is public record; whether it can supply you today is a conversation you have with the facility, against your own policy.

See who reported compounding a substance

Live shortage status, the 503B facilities that reported compounding it to FDA with the reporting window on every row, and each facility's documentation standing. Whether any of them can supply you today is a conversation you have with the facility. Included on the Clinic plan.

Inspection readiness

Your documented coverage right now

Know today how much of a records request you could hand over, so an inspection is a print job instead of a panic.

Coverage % right nowRecall DrillDaily coverage snapshotsOne-click binder
Record coverage coverage counts against named references, never a compliance determination

Storage

Every check you run is kept as a durable dated record, searchable by product, supplier, lot or file name, so any one of them is a search away years later. The record and the original file you uploaded are separate things: the record is always kept, the original artifact is not always retained. Each row states its own state, and the retention matrix below says which is which.

Record durable on any planSearch by product, supplier, lot, fileCSV exportOriginal file: state shown per row
Storage
RecordDocumentSupplierResultDatePDF
What is retained artifact by artifact, so “stored” means one thing
Retention state by artifact class. Where a class varies by record, the row in the table above is authoritative.
ArtifactWhat it isRetention state
Check recordIts id, product, supplier, lot, dated result band and flag countKept for the life of the workspace, on every plan
Extracted fields and findingsWhat the engine read off the document, and what it concluded from itKept with the record
Generated report PDFThe rendered one-pager for that checkRe-downloadable while the record carries one. A record with no PDF shows a dash in the PDF column and can be re-run to produce one
Original uploaded fileThe exact file you dropped inRetained for checks run on a paid workspace. Where it was not retained, the row’s document icon is dimmed and the file route answers that no original is retained. Not every record has one
Evidence and audit eventsWho ran what, when, and what changed afterKept on the workspace journal, which is a separate record from this table
ExportEvery row of the table above, as CSVOn demand, from Export CSV on this page

Nothing outside these rows is a retention promise. Backup, restore, legal hold and deletion handling are deliberately absent because this page does not implement them.

Sourcing receipts
Audit-ready binder one click, inspector-ready

Facing an FDA or board records request? Pull every saved check and order-level Evidence Passport on file into one organized, inspector-ready PDF. Documentation evidence only.

Generate audit-ready binder
Audit-ready binder Clinic plan

Compile every saved check and Evidence Passport into one inspector-ready PDF for an FDA or board records request. Included on Clinic ($99/mo) and the Supplier program. Your saved checks below are yours on any plan.

Collect a COA from a vendor

Send a supplier a private upload link. No account needed on their end. What they upload is checked and saved to your storage above automatically.

Collect a COA from a vendor Paid plans

Send suppliers a private upload link and collect their certificates straight into your storage. Available on any paid workspace.

Monitoring

Your supply base re-checked continuously, so a recall or enforcement action reaches you as an alert instead of a surprise.

Enforcement + recalls watchedFormulary eligibility re-checksEmail alerts on changeEvery sweep on the record
Suppliers monitored
0
Open alerts
0
Last scan
Auto re-check
Lot Recall Net matched by lot number, across the whole network
Loading your recall-net coverage…
Formulary eligibility your lots vs the current FDA lists, live
Supplier risk Ranked by documentation risk on file
Watch & alerts
Scan activity every sweep, on the record

Continuous monitoring + alerts

Suppliers don’t stay clean forever. We re-check them and alert you when a new packet, signature, or source signal appears.

Evidence Passport

Portable, customer-safe proof of the diligence you performed, so your work travels with the order instead of staying in your files.

Issued only while a lot is clearedVerifiable at one public linkCustomer-safe by design
How this reaches the patient pick the channels this run produces, then issue below
Step 1 · every channel starts hereIssue the passports per customer order, or one reusable supplier-level proof

Issue an Evidence Passport per customer order (one or many at once), or one reusable supplier-level proof of a lot's diligence. Sandbox records are free for testing; production order release requires a payment method, first production Passport on us, later order releases at $3 per order, or $0.50 on a committed-volume agreement (500+/month) (custom rate for high-volume platforms); supplier-level passports are included free with your credential. Document diligence only; no quality, safety, or approval claim.

Drop or paste today’s shipment export straight in. A row’s own lot overrides the lot picked above, so a mixed-lot day works in one paste. An email on the row means that order is ready to send. Patient names and addresses are read in your browser and never sent to Veritura.
In the bag · printable slipPrint bag slips for orders that already have a passport, including reprints

One slip per order: the order number large, with that order's own verify QR. Paste the order numbers, one per line. Nothing is issued or billed here, these are the passports you already have.

At the benchPack a run scan the packing slip, everything else follows

A scan of an order that already has a passport reuses it, never re-bills. Printing follows the channels selected above: vial labels, bag slips, or both. Order numbers only, never patient details.

On the vial · printed QRVeritura Seal the physical product: a serialized QR sticker you print and apply to the vial
Shipping to orders

Order-bound, from the composer

Issuing passports with this channel on mints one seal per order, with the ORDER number printed on the sticker. Match sticker to packing slip; the patient’s scan shows their own order back to them.

Sealing stock

Label a lot before orders exist

From any lot record: up to 500 lot-level labels at a time, printed as Avery 5160 sheets, a thermal roll, or raw ZPL straight to your label printer. The API mints them from your own system too.

The patient’s side

A vial they can save

Scanning opens that unit’s record. Patients can save their vial with just an email, and if a recall notice ever reaches the lot, one button notifies every saved vial. We never receive patient names, addresses, conditions, or prescribers; a patient who saves a vial gives only an email and that vial’s serial.

See the patient space →
Bind an already-printed seal to an order

For seals printed before you knew the order, from a roll of blank stock. One line per vial: the code on the seal, a comma, then the order number. Order numbers only, never patient details.

Try the Passport workflow in sandbox

Create free sandbox records to see the order-to-lot proof structure. Activate production when you are ready for customer-safe release; the first production Passport is complimentary.

Verified Supplier

Build the six-element qualification profile once and publish one verify link, so every buyer conversation starts from evidence instead of a sales claim.

Six verifiable elementsFDA registration matched at sourceOne verify link + embeddable badgeYou choose what to publish

Check ad copy

Paste your ad copy or landing page text. See which claims are checkable with documentation evidence, which need reframing, and which cannot be backed.

Documentation evidence onlyReframe suggestions, never legal advice
Step 1 · Tell us about this ad all optional, and it sharpens the disclosure + routing map
Loading questions…
Step 2 · Paste your ad copy or landing page text an automated first pass on the wording, not legal advice

Claim register

Keep every advertising claim backed by documentation evidence, and know the day the evidence behind one changes.

Dated substantiation historyBound to live evidence objectsDocumentation evidence only
Documentation evidence only. Not legal advice.

Settings

Your organization, plan, team, and the policy that governs every decision this workspace signs.

Policy & autonomyTeam seatsMorning digestAPI keys & webhooks

Organization

Company
Work email
Facility type

Your desk organizes the whole workspace: which tools lead, how the pipeline reads, and the plan we recommend. Everything else stays one click away under More.

Label brand name

Printed as the top line on your vial seal labels and shown as “Dispensed by” on the public scan page. Leave blank to use your company name.

Patient contact

Shown to patients on the public record page for the medicine you dispensed, under “Questions about your medicine”. A phone number or email becomes a tap-to-call or tap-to-email link on a phone. Leave blank and the page names your pharmacy without publishing a contact route. Never taken from your login email.

Show all features

On, the sidebar stays flat and nothing collapses into the More group. Off, features that are secondary for your facility type tuck into More at the bottom of the sidebar. Every feature stays available either way.

Plan & billing

Current planFree plan
Suppliers covered
RenewsMonthly
Manage plan

Team & seats

Seats used1 seat

Add teammates who share this workspace on the Clinic plan ($99/mo).

Security

DocumentsAccess-scoped storage
AccessScoped + logged
Release authorityYour signed ClearGate policy

Morning digest

An overnight brief scoped to YOUR suppliers and lots: new FDA enforcement/recall signals, monitoring alerts, flagged lots, overdue file reviews. Sent at most once a day, and only when there is something real to say.

Send after (UTC hour)

Payment method checking…

Evidence Passports are billed monthly for the orders you released. This is the card that gets charged.

Autopilot checking…

Fully autonomous means: orders arrive on their own, passports release themselves under your policy, patients get their record without anyone clicking send, and you read one digest of anything that needs you. These four switches are the whole setup.

Every autonomous release stands on the same floor as a manual one: a cleared lot, no hold, no recall signal, your policy satisfied, and the billing gate in front. Nothing here weakens a gate.

Developers · API & webhooks

Moved to its own page: API in the sidebar, under Account. Test keys, live keys, the metered passport key, and webhooks all live there now.