United States
FDA MoCRA
Facility registration, product listing, and adverse-event posture are handled by the Compliance agent.
Tinctloom · Manufacturing cloud
The AI manufacturing cloud for the global beauty industry. Formulating, sourcing, certifying, producing and scaling — collapsed into one workspace that runs on smart contracts and live quality telemetry.
The status quo
Today, launching a beauty product means threading contract-manufacturing portals, supplier emails, agency retainers, certification portals and a quality spreadsheet — each with its own login, its own audit trail, and its own hand-off deadline.
Tinctloom replaces that stack with one programmable workspace where each step has a single owner and the boundaries between them are signed, not improvised.
The platform
Each capability is an independent surface of the platform; every one of them already speaks to the others, so a brand, a manufacturer, a supplier and a certifier can move through a launch without rebuilding the boundary in between.
01 — Formula
R&D agent drafts INCI-ordered compositions against your brief, with stability, sensory, and allergen scores already cross-referenced.
02 — Source
Sourcing agent ranks GMP-certified suppliers by ledger-anchored transparency, MOQ fit, and lot-to-lot COA integrity.
03 — Evidence
Every batch, cert, and signature settles to an L2 rollup — auditable end-to-end, on demand, across markets.
04 — Pipeline
QC agent reads pH, viscosity, and fill weight from the line; Brand Builder ships storefront, label, and packaging in the same run.
Multi-agent system
Tinctloom assigns each decision to an agent with a single responsibility. Pick an agent to see what it outputs, what it signs, and which agent it hands the work to next.
Output
Drafts ingredient composition with claimed skin-feel, INCI-ordered text, and a stability score. Cross-references the supplier library for sensitivities before a hand-off.
Launch workflow
The same launch that used to bounce across portal logins, spreadsheets and email threads now moves through five signed states. Each state has an owner. Each hand-off is logged.
Brief the platform. The R&D agent drafts three formulas against your sensory + claim targets.
Compliance agent clears each draft for FDA MoCRA, EU 1223/2009 and ISO 22716 before it leaves the lab.
Sourcing agent picks rank-1 suppliers; the brand-builder packages your label, claims and storefront copy.
QC agent ingests line telemetry in real time; every checkpoint writes to the compliance ledger.
Factory agent books the line, posts a smart contract, and pays suppliers when the QC checkpoint clears.
Compliance posture
Every launch on Tinctloom carries the same auditable evidence chain — from formula lock onward — that the majors operate. Auditors pull the trail in one query.
United States
Facility registration, product listing, and adverse-event posture are handled by the Compliance agent.
European Union
INCI declaration, allergen and CMR posture, and the Responsible Person hand-off sit inside the same workflow.
Manufacturing
Production, quality, documentation and deviation handling are reconciled to the standard at every QC checkpoint.
Frequently asked
Pilot cohorts are open now. Direct the harder questions to [email protected].
Plan your first launch
Whether you are an indie brand shipping your first SKU or a contract manufacturer integrating a new line — Tinctloom fits the workflow that already exists in your head.
We respond within one business day.