AI-powered compliance validation, annotation, and approval workflows—all in one place. Ask the built-in AI assistant anything about your portfolio, in plain English. Built for pharma, cosmetics, nutraceuticals, FMCG, and every regulated industry in between.
Every company managing product labels faces the same chaos. Version control. Approval delays. Compliance gaps.
Multiple artwork versions scattered across emails, WhatsApp, and drives. No single source of truth.
Manual routing through QA, Regulatory, Marketing, Legal stretches 2-3 week approvals.
Approvals happen in emails. No record of who approved what, when, or why.
Manual verification of labels, ingredients, warnings, and regulatory requirements. Human error kills launches.
A built-in AI with full read access to your compliance portfolio — across every product line and regulated category. No dashboards to click through. No reports to pull. Just ask.
What's blocking AW-7742-v3 from approval?
2 blocking issues found on AW-7742-v3:
Missing allergen warning for Peanut Oil — affects EU, US, ALL regions.
Tartrazine (E102) warning absent from panel 3 — affects EU.
Compliance score: 64 / 100. Approval blocked until CRITICAL issues are resolved.
Which artworks across our FMCG and cosmetics range need attention this week?
5 artworks need attention across 2 product lines:
Read-only · Action support coming soon
Ask about artwork status, compliance scores, version history, or workflow SLAs across pharma, FMCG, cosmetics, and more — in plain English.
Surfaces blocking issues, severity breakdowns, and remediation guidance across your entire portfolio — whether it's a drug label, a cosmetics pack, or a food product.
Compliance distributions, approval timelines, and SLA reports rendered as charts inside the conversation — no separate dashboard needed.
Route approvals, resolve annotations, and trigger compliance checks — directly from the chat window, across every product category.
Every feature is AI-augmented from day one. Compliance checks, version diffs, copy accuracy, and approval reports—all driven by LLMs with a full audit trail.
Mark up artwork directly on screen. Pinpoint corrections, track all changes. Every annotation is logged—no lost comments, no scattered WhatsApp threads.
Design workflows that match your process. Route through QA, Regulatory, Marketing, Legal. Parallel or sequential. SLA enforcement with escalation.
Configurable rule sets across FSSAI, CDSCO, EU Cosmetics Regulation, and FMCG labelling standards. AI evaluates every text-verifiable rule; visual-only rules are flagged for human review. Scores every artwork out of 100.
Compare artwork versions field by field. Check copy accuracy against master manuscript. Generate approval reports as PDFs. OCR extraction powered by a Python sidecar.
Arcwork was built for regulated industries. Every feature—audit trails, approval workflows, e-signatures—is designed to meet global compliance standards: FDA, EMA, FSSAI, and more.
All artwork versions are digitally signed, timestamped, and instantly exportable for regulatory review.
Automated validation of mandatory declarations against regional schedules.
Join our beta program. Get hands-on access to annotation, workflows, and AI-powered compliance checks for your industry.
Get hands-on access to Arcwork months before general availability.
Your feedback directly influences features, integrations, and compliance configurations.
Lock in lifetime founder pricing—up to 20% off standard rates.
Direct line to the founding team for onboarding, training, and technical questions.
We're admitting beta partners in waves. Join the queue and we'll reach out when it's your turn.
We're looking for 5-10 teams to pilot Arcwork and help shape its future. Pharma, cosmetics, nutraceuticals, FMCG — any industry managing artwork approvals. You get founder pricing and direct input on the product.
Tell us about your team and workflow. We'll reach out to schedule a call.