MAATIQ AGENT WORKBENCH

AI proposes. You decide.

A review workbench for FDA compliance consultants: AI lays out every finding with its CFR basis and source evidence, and you adjudicate each one from the keyboard. Ten times the review throughput, and the signature is still yours.

Create a free account Book a 15-minute demo

Includes a demo review. Try it in 5 minutes.

Every finding traces back to its source

Click a finding and the left pane highlights the exact label text it cites, while the right pane shows the CFR citation and the AI confidence score. Defensibility is not a slogan: every single finding carries an evidence chain.

LABEL SOURCE

Citrus Vitamin C Gummies

INGREDIENTS: Glucose syrup, sugar, pectin, sodium citrate, natural orange flavor, ascorbic acid.

Supports healthy immune function and prevents colds.

Distributed by Sunrise Wellness Foods, Taoyuan City.

FINDINGS

MAJORAllergen statement placement

BLOCKINGUnauthorized health claim

Disease-prevention claim on a conventional food label without FDA authorization.

MINORNet quantity type size

REGULATORY BASIS

21 CFR 101.14(a)(1)

Health claims characterizing the relationship of a substance to a disease require FDA authorization before use on food labels.

AI CONFIDENCE

0.94

Keyboard throughput, not mouse-clicked cards

J/K to move, A to accept, R to reject, M to modify, N to add a missed finding. A few keystrokes clear a finding, and clearing a whole submission takes minutes.

The report you deliver is yours

Co-branded PDF: your firm's name, your signature, and only the items you have adjudicated. Unreviewed AI proposals never appear in front of your client.

DEVICE 510(k)

The medical device line is live

The same consultant adjudication workbench now supports pre-submission review for FDA 510(k) medical devices.

Create a free account

RTA acceptance screening

Automatic checks across 43 510(k) RTA / eSTAR technical screening items to catch administrative and format gaps before hold.

Pre-Sub question quality review

Checks whether Q-Submission questions are specific and answerable by FDA, with gaps around predicate strategy, clinical evidence, and cybersecurity files.

$0.10 / 80 seconds per case

Cost and speed calibrated from a measured device run: about $0.10 and about 80 seconds for the initial findings.

How it works

1
Upload label photos and OCR fills the form automatically
2
Multi-layer AI review produces findings, each with severity, CFR citation, and source evidence
3
You adjudicate line by line and generate a report under your name in one click

The three things consultants care about most

Your client data belongs to you alone

Organization-level isolation and a full audit trail (who, when, what changed; exportable).

AI does not sign. You sign.

By design, no finding enters any report without your adjudication.

What was reviewed, and on what basis

Every report includes a methodology note and a consolidated index of CFR citations.

Precios

Prueba el workbench completo gratis durante 30 días y luego elige tu plan.

Trial

El workbench completo con casos reales, sin datos de pago.

Gratispor 30 días

Todos los módulos: alimentos, cosméticos, 510(k), Pre-Sub
10 revisiones incluidas
1 informe GRAS/NDI incluido
Sin tarjeta de crédito

Empezar 30 días gratis

Recomendado

Pro

Para consultores que revisan expedientes de clientes cada semana.

$299por asiento / mes

25 revisiones por asiento al mes
Módulos de alimentos, cosméticos, 510(k), Pre-Sub
Informes GRAS/NDI a $199 cada uno
Informes PDF co-brand con tu nombre
Soporte por correo

Enterprise

Desde 5 asientos, con contrato anual.

$999+al mes

Volumen de revisiones a la medida del equipo
Informes de marca blanca
Acceso a API
Soporte prioritario

Reservar una demo

Precios en USD. Como referencia: una revisión de etiqueta hecha a mano suele partir de $250.

Frequently asked questions

Will the AI mislead my judgment?: The AI only proposes. Every suggestion comes with a confidence score and source evidence, and you can reject it with one key. Your rejection history also tunes the system to your review standards over time.
Which regulatory scopes are supported?: FDA food labeling, cosmetics MoCRA, and GRAS/NDI notifications. More regulation modules are planned.
Will client data be used for training?: Adjudication statistics are used only in de-identified form to improve review accuracy, and never include client names or product identifiers.