TSCA reporting
Find out what TSCA requires for each substance you make in or import into the US.
ProjectsTSCA reporting
- Hollis Marsh
- Danielle Brooks
- Raj Patel
| Substance | Inventory | Status |
|---|---|---|
| Trichloroethylene | Active | Banned |
| 6:2 FTSA | Active | To report |
| 4-(Trifluoromethyl) | Inactive | Notice first |
| DCTF | Active | SNUR |
| N-Methylpyrrolidone | Active | Rule proposed |
| 2-Methyltetrahydrofuran | Active | CDR only |
6:2 FTSA PFAS rule
Status: To reportReporting opens by 31 January 2027
- Test
- Meets a structure in 40 CFR 705.3
- Sooner if
- 60 days after EPA’s revised rule
- Threshold
- No volume threshold, unlike CDR
Your expert signs off every substance
You get the TSCA register, a calendar of each report and notice, and the source behind every status.
Approval
Illustrative projectHollis Marsh
Status: ApprovedDirector of Regulatory Affairs, after checking each substance against all 5 TSCA requirements
Inventory status
Chemical Data Reporting
PFAS reporting rule
Section 6 rules
Significant new use rules
Foresight does the research
Your team brings what only it knows, and your expert makes the call at each checkpoint.
Tasks
Status: In progressIllustrative project3 of 5 tasks done.
Share your substances
Your team
Status: DoneDraft the checks
Foresight
Status: DoneAgree the checks
CheckpointStatus: ApprovedHollis Marsh
Check every substance
Foresight
Status: In progressApprove the register
CheckpointStatus: Not startedHollis Marsh
Kept current once it’s approved
Monitoring watches the rules behind your register. When one moves, Foresight rechecks the substances it affects, and your expert reviews the change.
Monitoring
Illustrative projectWatching 4 measures behind the register
- Status: To review
US TSCA section 8(a)(7) PFAS rule
EPA set the start of reporting to 31 January 2027, or 60 days after its revised rule if earlier. Rechecked, still to report.
Chemical Data Reporting, 40 CFR part 711
Proposed section 6 rule for NMP
TSCA Inventory, active and inactive listings
What we need from you
Four things, shared at setup before the project starts.
Your substances
What you make in or import into the US, with CAS numbers and uses.
Your volumes
Yearly volumes for each US site: from 2011 for anything fluorinated, since the PFAS rule covers every year from 2011 to 2022, and from 2024 for CDR.
Your priorities
What’s most urgent for you, such as a reporting window or a planned first import.
Your approver
The person who agrees the checks and approves the register.
What teams ask about this project
How do you decide which CDR threshold applies?
From each substance’s TSCA status. CDR’s threshold is 25,000 lb a year at a site, or 2,500 lb for a substance that is the subject of a proposed or final section 6 rule, a SNUR or certain orders. EPA reads that status on the first day of the submission period, 1 June 2028, so Foresight records each substance’s rules as they stand and watches for changes.
Can’t we just check the TSCA Inventory ourselves?
You can, and the download is a good start: it shows whether each substance is active or inactive. Its regulatory flags lag, though. In EPA’s July 2026 Inventory, NMP carries no section 6 flag, although EPA proposed a section 6 rule for it in June 2024, and that rule lowers its CDR threshold to 2,500 lb. Foresight checks each substance against the rules themselves.
Where does the evidence come from?
From the rules themselves: the Code of Federal Regulations, the Federal Register, and EPA’s own guidance and Inventory files. Every status links to its source, so your team can check the wording directly.
Who checks the register before we use it?
The person you name. They agree the substances and checks first, and check each status against its sources at the end. Nothing is final until they approve it. These checks reduce the risk of error without removing it.
What happens when a rule changes?
Foresight rechecks the substances it affects, such as when EPA revises its PFAS rule or finalises a section 6 rule. The register your expert approved stays as it is until they accept the change.
What does it cost?
The price follows how many substances, sites and years the register covers. You see it with the scope, before any checking starts.
More ways to meet an obligation
Each runs the same way, with your expert approving the result.
- PPWR compliance programmePackaging requirements, milestones, and evidence in one plan.
- EPR reportingPackaging and product data prepared for each country’s EPR scheme and deadline.
- REACH registration dossiersEU and UK REACH registrations, from data gap analysis to a dossier ready to submit.
- CLP classification and labellingMixture classifications under CLP, and the label elements that follow.
- Poison centre notificationsCLP Annex VIII notifications, with a UFI for each mixture.
- SCIP notificationsArticles with Candidate List substances above 0.1%, prepared for ECHA’s SCIP database.
- Plant protection product dossierDossier evidence, ownership, and review status in one place.
- Biocidal product dossierProduct authorisation dossiers under the EU Biocidal Products Regulation.
Bring your substance list to a demo
Tell us what you make in or import into the US. You’ll see the scope and the price before any checking starts.
