Manufacturing
One spine from supplier document to SDS to shipped product.
ToxIntel gives manufacturing operations a governed Supplier → Raw Material → Lot → Formula → Batch → SKU → Market → SDS spine — with real change management, reviewer sign-off, and downstream-customer documentation flowing from the same record.
Where ToxIntel enters this work
The specific work this platform is built to serve.
- ◆Formula and material intake with supplier documents captured against a governed raw-material record — not attached to a shared drive.
- ◆SDS authoring inheriting hazard classification, exposure limits, transport, and regulatory posture from the same governed record.
- ◆Supplier documentation workflow — declarations, CoAs, SDSs, POPs statements, microplastic statements — tied to the raw material and to the lot.
- ◆Chemical inventory management across TSCA, DSL/NDSL, ECHA, AICIS status per substance.
- ◆Change management — a raw-material substitution automatically flags the batches, SKUs, and SDS revisions it triggers.
- ◆Downstream-customer documentation packages assembled once and delivered under the correct governance envelope.
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
Corporate Consciousness ERP — Supplier → Raw Material → Lot → Formula → Batch → SKU → Market → SDS spine, with Suppliers 16, Raw Materials 12, Lots 7, Formulas 12, Batches 7, SKUs 7 and the Market Release Signal (Release / Conditional / Blocked / Insufficient Data / Pending Review).
Open in ToxIntel →
Real, sanitized view · from the live platform
Central Scientific Review Console — SDS submissions queued with Overview / Formula / Classification / Draft SDS / Scientific Decision Log / Audit Trail tabs, and governed actions Scientifically Approve / Request Revision / Reject / Escalate.
Open in ToxIntel →
Real, sanitized view · from the live platform
Cross-Module Governance — every governed record is tied to the downstream modules that consumed it, so a change to a substance surfaces in every SDS, TRA, and QRA that depends on it.
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 / RM / Lot / Formula / Batch / SKU / Market / SDS bound into one governed spine per tenant, with bidirectional genealogy. |
| SDS Intelligence | Governed SDS drafts inherit hazard, exposure, transport, and regulatory records from the same substance dossier; every revision is auditable. |
| Scientific Review Console | Every SDS revision receives a scientific decision log, reviewer sign-off, and an immutable audit trail before release. |
| Supplier Documentation | Declarations, CoAs, and POPs/microplastic statements are captured against the raw-material record — not floating as email attachments. |
| Regulatory Intelligence | TSCA CDR, REACH RMOA, and jurisdictional inventory status attached to the substance and the SKU they affect. |
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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