New: Refreshed product demos for Netta IUCLID, Review and Cite. Watch them

Netta Tech

AI Software · Built in the EU

Finish in minutes what used to take your team days.

Regulatory documentation eats specialist hours: study plan reviews, IUCLID dossiers, literature searches, meeting minutes. Netta Tech handles the heavy lifting so your consultants, scientists and compliance teams can focus on the work only they can do. More consistent than manual review.

Netta IUCLID: from study report to IUCLID in minutes. See how it works →

Product benchmarks

Hours of specialist work, handed back.

per IUCLID dossier Netta IUCLID
Weeks → hours
less time per study review Netta Review
~85%
saved per substance data search Netta Cite
~8 h
to clean, fileable minutes Netta Minutes
2 min

* Internal benchmarks on representative documents.

What we work on

  • OECD GLP compliance
  • IUCLID dossiers
  • REACH registration
  • Biocides
  • Study plan review
  • Substance research
  • Meeting documentation
  • EU-hosted · GDPR-ready

Who it’s for

One suite for the people who sign off.

For regulatory consultancies

Take on more study reviews and dossiers without adding headcount. The system drafts and checks; your experts review and sign.

Talk to us

Output: graded findings

Netta ReviewCompliance findings
Netta Review: study plan findings graded and cited to the guideline

For in-house compliance teams

The same checks on every document, every time, with a reviewer signing off and your data kept in the EU.

Talk to us

Your workspace

Netta TechDashboard
Netta workspace overview

Our products

Five tools that give your team back the hours they spend on paperwork.

Each one handles a specific piece of regulatory or operational work. Your experts review the output. The system does the heavy lifting. More consistent than manual work, and your experts stay in control of the output.

  • IUCLID dossier assembly: weeks of data entry, handled.

    Preparing an IUCLID dossier means weeks of manual data entry across dozens of endpoints. Upload your study reports, get back populated endpoint entries, with the study report attached to each endpoint record. Your scientists review, the system drafts.

    Learn more →
  • Study reviews in minutes, not hours.

    Your team spends hours reviewing study plans and reports against OECD and ISO guidelines, and analytical methods against SANCO/SANTE. Upload the document, get back every finding: graded, cited to the exact guideline paragraph, ready for your reviewer to sign off. More consistent than manual review.

    Learn more →
  • Find out what data already exists for your substance.

    Before you send a substance to the lab, you need to know what information is already out there. Enter a CAS number or substance name. Netta Cite searches every endpoint (solubility, repeat-dose toxicity, ecotoxicity and more), extracts the key values (NOAEL, LOAEL, EC50...) and gives you a citation for each one. Know which tests you can skip before you spend the money.

    Learn more →
  • Meeting minutes your compliance team can file.

    Nobody enjoys writing meeting minutes, but in regulated environments they are mandatory. Upload your transcript, get structured Word minutes: attendees, decisions, action items, owners. Nothing stored, nothing retained.

    Learn more →
  • The right tone for every professional email.

    The wrong tone in a client email costs more than time. It costs trust. Paste your draft, pick a tone, get back a polished version. Same intent, better clarity. Built for non-native English speakers writing to regulators and auditors.

    Learn more →

Input: one study report per endpoint

Netta IUCLIDNew extraction
Netta IUCLID: IUCLID dossier assembly: weeks of data entry, handled.
  1. Endpoint type
  2. Study report for this endpoint
  1. Guideline paragraph cited
  2. What the study plan says
  3. Assessment in plain language
  1. Substance identity: CAS and EC
  2. Endpoint group with coverage status
  3. Value with its literature source
  1. Meeting date and length
  2. Summary
  3. Key decision
  1. Your original draft
  2. Rewritten in the chosen tone

Beyond the products

Custom systems, built like the products.

When the off-the-shelf answer doesn’t exist, we build it. Same standards, same opinionated stack, same hand-over guarantee.

01

AI Integration

Your board says “we need AI.” But where, and how, without breaking compliance? We find the use cases that actually save your team time, build them into your existing workflows, and make sure your DPO signs off. Not a chatbot on your intranet: real solutions for real bottlenecks.

02

Data Organisation

All your data in one place, structured and connected, from lab results to financial reports. Clean dashboards your management team can actually use, with a full audit trail. No more chasing spreadsheets across shared drives.

03

Internal Tools

Every organisation has processes that live in spreadsheets, emails and people’s heads. We turn those into proper software (admin panels, knowledge bases, automated workflows) so the work gets done even when the one person who knows how is on holiday.

04

Advisory & Audits

Not sure where to start? We run AI readiness assessments, help you pick the right vendors, review your security posture and prepare you for audits. Sometimes the right answer is to do less, slower. We’ll tell you that too.

How we work

Four promises we put in writing so you can hold us to them.

  • 01

    Everything we sell is live today.

    Every product on this site is in production with real users. You can book a demo this week and see your own documents processed. No roadmaps, no waiting lists.

  • 02

    More consistent than doing it by hand.

    Our tools check every item on the list, every time. No Friday-afternoon shortcuts, no reviewer fatigue, no missed paragraphs. Your experts review the output and sign off. The system never skips a step.

  • 03

    Your data stays in the EU.

    Our software runs on EU servers, in EU jurisdiction. Nothing is used to train models. If your compliance team prefers the software on your own hardware, we can deploy it there.

  • 04

    Findings you can verify.

    Every Netta Review finding cites the guideline paragraph it rests on. Every Netta Cite value cites its source. When an auditor asks “where did this come from?”, you have the answer.

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.