Consumer Products
Product stewardship across the portfolio — not one SKU at a time.
ToxIntel connects supplier documentation, formulation records, safety assessments, regulatory obligations, claims files, and retailer readiness so a consumer-products team can see the whole portfolio and act on it before the market does.
Where ToxIntel enters this work
The specific work this platform is built to serve.
- ◆Formulation and material intake connected to supplier documents, SDS records, and the governed ingredient dossier.
- ◆Portfolio-wide safety-status view — every product tagged with its current scientific readiness, reviewer, and outstanding actions.
- ◆Regulatory-change surveillance flowing directly into the products the change affects — not into a separate inbox.
- ◆Claims files tied to the scientific evidence that substantiates them, in the state your Legal team can defend.
- ◆Executive risk view across MoCRA action-required signals, retailer alerts, restricted-substance changes, and reformulation triggers.
- ◆Portfolio triage for external partner requests — one place to receive, quote, and route incoming work.
Inside ToxIntel
See the technology behind the workflow.
Real, sanitized views from the live ToxIntel platform — no mockups, no fabricated data. Each screen below is what an authorized toxicologist, brand safety lead, or retailer reviewer actually works with every day.
Real, sanitized view · from the live platform
Product Safety Intelligence library — every project with formula metrics, regulatory snapshot (FDA MoCRA action required, EU 1223 pending, IFRA in review, Prop 65 in review), and reviewer status.
Open in ToxIntel →
Real, sanitized view · from the live platform
Portfolio Request Triage — 292 external requests staged Pending / Reviewing / Quoted / Approved / Fulfilled / Rejected. Full auditability for cross-team work.
Open in ToxIntel →
Real, sanitized view · from the live platform
Cross-Module Governance — every governed scientific profile with every downstream consumption event across TRA, SDS, QRA, Claims, Retail, Regulatory, Prop 65, Medical Device, Stewardship, Compliance Passport, and Ingredient Copilot.
Open in ToxIntel →Every deep-link requires ToxIntel sign-in. Request an enterprise demo above and we'll walk you through them on live records.
What it maps to
Existing capabilities → where they enter your workflow.
| Existing capability | Where it enters your workflow |
|---|---|
| Product Stewardship ERP | Supplier → Raw Material → Lot → Formula → Batch → SKU → Market → SDS is one persisted, auditable spine per tenant. |
| Portfolio Request Triage | Every incoming safety, regulatory, or claims request is staged, assigned, and closed in the same system that generated the work. |
| Regulatory Intelligence | Regulatory changes are attached to the ingredients, formulas, and SKUs they actually touch — not delivered as a bulletin your team has to reconcile. |
| Cross-Module Governance | Every governed profile records the downstream modules that consumed it — proof of reuse instead of hidden duplication. |
| Executive Command | Portfolio-level KPIs (active formulations, submissions, claims, retailers, open hazard alerts, reviews) surfaced for cross-functional leadership. |
Business outcomes
See how it fits your team.
A 30-minute session on live records — no slides. Bring the workflow question you actually need answered this quarter.
Shared core capabilities applied in this workflow
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