REACH registration dossiers
Prepare your EU and UK REACH registrations, from the data gap analysis to a dossier ready to submit.
ProjectsREACH registration dossiers
- Mirela Dunstan
- Florian Weber
- Yasmin Aziz
| Substance | Deadline | Data gap | Status |
|---|---|---|---|
| AEEA | 27 October 2029 | Exposure assessment | Gap |
| Cocamidopropyl betaine | 27 October 2030 | Waits on the ATRm | Not started |
| Isopropyl myristate | 27 October 2031 | Physicochemical data | Not started |
| DMCHA | 3 months after reaching 100 t | Annex IX data | Gap |
| Isopropyl palmitate | Before first import | Physicochemical data | In progress |
| Lauramine oxide | None due | None | Registered |
AEEA UK REACH
Status: GapRegister by 27 October 2029
- Hazard
- Repr. 1B on the GB MCL list
- Requires
- Exposure assessment and risk characterisation
Your expert signs off EU and UK REACH
You get the registration plan, the data gap analysis for each substance, and each dossier drafted in IUCLID’s format.
Approval
Illustrative projectMirela Dunstan
Status: ApprovedHead of Product Stewardship, after checking every deadline and data gap under both regimes against their sources
EU REACH
UK REACH
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 registration plan
Foresight
Status: DoneAgree the plan
CheckpointStatus: ApprovedMirela Dunstan
Close the gaps and draft
Foresight
Status: In progressApprove the dossiers
CheckpointStatus: Not startedMirela Dunstan
Kept current once it’s approved
Monitoring watches the measures behind your registration plan. When one moves, Foresight rechecks the substances it affects, and your expert reviews the change.
Monitoring
Illustrative projectWatching 4 measures behind the plan
- Status: To review
UK REACH transitional deadlines, Article 127P
SI 2026/849 moved the deadlines from 2026, 2028 and 2030 to 2029, 2030 and 2031, from 6 August 2026. Rechecked, AEEA is now due 27 October 2029.
UK REACH alternative transitional registration model
EU CLP new hazard classes, Delegated Regulation (EU) 2023/707
UK REACH candidate list
What we need from you
Four things, shared at setup before the project starts.
Your substances
The substances you make or import, with their CAS numbers or safety data sheets.
Your tonnages
How much of each you import a year in the EU and GB, and the registrations, DUINs and letters of access you hold.
Your priorities
What’s most urgent for you, such as a new import or a customer moving to a higher band.
Your approver
The person who agrees the registration plan and approves the dossiers.
What teams ask about this project
How do you find the data gaps?
From each substance’s tonnage band. REACH asks for Annex VII data from 1 tonne a year, Annex VIII from 10, and testing proposals for Annex IX from 100 and Annex X from 1,000, with a chemical safety report from 10 tonnes. Foresight marks what you hold, what the joint submission can share, what can be waived with a justification and what needs a test or a testing proposal.
Where does the evidence come from?
From the regulations themselves: REACH and its annexes, UK REACH as legislation.gov.uk publishes it, the EU’s rules on dossier updates, and the regulators’ own guidance. Every deadline and gap links to its source, so your team can check the wording directly.
Should we buy data for UK REACH now, or wait for the ATRm?
It depends on the substance. The government’s draft alternative transitional registration model, the ATRm, would let a GB registrant of a substance registered in the EU at the same band or higher submit hazard conclusions in place of the study data. Its technical consultation closes on 10 November 2026, and it isn’t law yet. A substance in Article 14(4)’s hazard classes, such as a Repr. 1B amine, still needs its own exposure assessment under the draft, so that work can start now.
Who checks the dossiers before we submit them?
The person you name. They agree the tonnages and deadlines before any drafting starts, and check every dossier 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, as when the UK REACH deadlines moved in August 2026. The plan your expert approved stays as it is until they accept the change.
What does it cost?
The price follows the plan’s size: how many substances, regimes and tonnage bands it covers, and how much data you already hold. You see it with the scope, before any drafting 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.
- 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.
- TSCA reportingInventory status, CDR and PFAS reports for substances you make in or import into the US.
- 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 tonnages to a demo
Tell us your substances and whether you make or import them in the EU, GB or both. You’ll see the scope and the price before any drafting starts.
