Netta IUCLID
IUCLID dossiers assembled — REACH, biocides and CLP.
Netta IUCLID automates IUCLID dossier assembly for REACH registration, biocides authorisation and CLP notifications. It parses endpoint study reports, populates IUCLID 6 v9 fields, cites every value back to its source page — and hands a clean dossier to a scientist for the last-mile review.
Weeks → hours
per IUCLID dossier
149
endpoint types covered
REACH · BPR · CLP
three regulations, one tool
Regulatory scope
-
REACH Annex VII–X
Registration dossiers
-
BPR (Biocides)
Active substance + product authorisation
-
CLP
Classification & labelling notifications
-
IUCLID 6 v9
Current ECHA schema
-
i6z export
Manual upload path
-
IUCLID server push
Direct integration
How it works
From a stack of study PDFs to a validated i6z dossier.
- 01
Drop the study PDFs
Upload endpoint study reports — OECD, EPA, in-house — in any language the regulator accepts. We parse the structure, the tables, the summaries and the robust study summaries.
- 02
Endpoints auto-populated
Every relevant IUCLID section and field is filled from the source study. Material, method, results, reliability, key study flag, reference — all extracted and structured for review.
- 03
Reviewer in the loop
A scientist reviews each populated endpoint with the original study open alongside. Nothing is finalised without human sign-off.
- 04
Validate and export
Built-in IUCLID validation rules run before export. Push directly to your IUCLID 6 v9 server, or export an i6z dossier for manual upload to REACH-IT or R4BP 3.
Every extracted value carries a citation back to the source study and the exact page. No field is invented. Reviewers accept, correct or reject — the tool never signs off on its own work. More consistent than manual review — the system checks every item, every time. No reviewer fatigue, no missed paragraphs.
Endpoints covered
The whole hazard profile, not just the easy bits.
Physical-chemical
- Melting / freezing point
- Boiling point
- Relative density
- Vapour pressure
- Water solubility
- Partition coefficient (log Kow)
- Surface tension
- Flash point
- Auto-ignition
- Granulometry
Toxicology
- Acute toxicity (oral / dermal / inhalation)
- Skin & eye irritation
- Skin sensitisation
- Genetic toxicity (Ames, MNT, chromosomal)
- Repeated-dose toxicity
- Reproductive & developmental
- Carcinogenicity
- Toxicokinetics
Ecotoxicology
- Short-term toxicity — fish, daphnia, algae
- Long-term toxicity — fish, invertebrates
- Sediment organisms
- Terrestrial organisms
- Activated sludge
Environmental fate
- Ready biodegradability
- Hydrolysis
- Adsorption / desorption
- Bioaccumulation
- PBT / vPvB assessment
Deployment
Your compliance team picks where the data lives.
Cloud
EU-hosted SaaS
- Hosted in the European Union
- LLM inference in EU regions under enterprise DPA
- Contractual prohibition on training on client data
- Onboarding within the week
On-premise
100% air-gapped
- Runs entirely inside your network — no outbound calls
- Netta custom models, tuned for IUCLID extraction
- Your data never leaves your infrastructure
- Compatible with hardened, disconnected environments
On-premise deployments run on Netta custom models tuned for IUCLID extraction. Nothing — queries, documents, extracted values — ever leaves your network.
Why Netta IUCLID
Built for the whole dossier, not just one regulation.
- REACH, Biocidal Products Regulation and CLP — all three in one tool
- EU-hosted SaaS or fully air-gapped on-premise — your compliance team decides
- 149 endpoint types across physical-chemical, toxicology, ecotoxicology and environmental fate
- No artificial page caps, no per-user metering, no lock-in
- Part of the Netta product suite — combine with Netta Review and Netta Cite for the full dossier workflow
Questions
The ones a reviewer would ask first.
If yours isn’t here, a 30-minute demo is the fastest way to get it answered. We don’t do gated whitepapers.
Book a demoWhich IUCLID version do you support? +
IUCLID 6 v9, the current ECHA release. We track schema updates as ECHA publishes them. Dossiers exported from Netta IUCLID validate against the current format checker.
Does it handle biocides (BPR) as well as REACH? +
Yes. Netta IUCLID covers REACH Annex VII–X registration dossiers, Biocidal Products Regulation active-substance and product-authorisation dossiers, and CLP notifications.
Where does the data live? +
On the SaaS tier, application and LLM inference run in the European Union under contractual terms prohibiting use of your data for model training. On the on-premise tier, nothing — documents, extracted values, queries — leaves your network.
Can it push directly to an IUCLID 6 server? +
Yes. Direct push is supported, and i6z export is always available as a manual path.
What study formats do you accept? +
PDF study reports in any language the regulator accepts. OECD test guideline reports, EPA studies, in-house laboratory reports and legacy scans with OCR.
Who does the work — the system or a human? +
The system drafts every endpoint from the source studies. A scientist reviews each one and signs off. Nothing is finalised without human approval.
How do you prevent hallucinations in a regulatory context? +
Every extracted field is grounded in the original study. Values without a defensible source are flagged, not invented. The reviewer always has the final say.
How long is onboarding? +
Cloud tier: production within the week. On-premise: timeline depends on your infrastructure, typically two to four weeks.
Get in touch
Ready to see it work on your documents?
Book a 30-minute call. No slides — we run your real documents through the system and you see the output. If it does not save you time, we will tell you.