One structured record, from first experiment to shipped product.
Uncountable is the connected ELN, LIMS, QMS, PLM and regulatory platform for materials and formulation teams. Change an ingredient in the lab and it's traceable through specs, QC release and production, with no re-entry and no reconciliation.
Deployed by 175+ enterprise product development teams
Deployed by Enterprise R&D and Innovation Teams
One data model, from lab to launch.
Most R&D organizations stitch product development together from tools that were never designed to talk to each other. Uncountable replaces each of them with a suite on the same data model, so the connections are built in, not bolted on. And it's configured to your workflow, without code.
Research & Development
Product Lifecycle
Regulatory Management
Project Management
Replacing a legacy ELN or LIMS?
Proof from the companies running it
When R&D, quality, product lifecycle, regulatory and project management share one data model, the payoff shows up as experiments never repeated and time given back to scientists.
CTO, Cooper Standard
CTO, Sun Chemical
46%
faster formula reviews, saving 34 hours each
15%
less materials waste = more sustainable R&D
1,000+
users across 35+ global sites
>50%
faster transition from testing to results
See the platform in action
How Clariant connected synthesis, formulation, testing, and commercial workflows to create an AI-ready R&D data foundation across 1,000+ users at 35+ global sites
Shared by every suite
Bodie and the Portal work across R&D, Quality, Product Lifecycle, Regulatory Management and Project Management at once, on the same structured data model.
Bodie, the AI Layer
The Uncountable Portal
Follow one formulation from lab to launch
Trusted by R&D and innovation leaders to capture every experiment, connect it to formulation and quality, and stop losing institutional knowledge when a project goes on the shelf.
- Capture and search every experiment: The ELN works like a searchable notebook, not a filing cabinet: graphing, reporting, and stats built in, so nothing gets lost between projects.
- Design fewer, better experiments: DOE & Predictive Tools plan multi-variable tests statistically, aiming for the most learning from the fewest runs, not one variable at a time.
- Carry context forward automatically: A formulation built in R&D carries its full history into quality and production, no re-entry, no lost context when it changes hands.
Every experiment captured, searchable and ready to reuse, so the next formulation starts from everything you already know.
Trusted by quality and QC leaders to catch out-of-spec results early, close the loop from event to root cause, and stay audit-ready without the scramble.
- Track failures, not just the final result: QC Lab keeps a full history of every retest, so a result never silently overwrites the one before it.
- Close the loop between events and evidence: Every CAPA, deviation, and change control links back to the formulation revision, batch, and raw-material lots that explain it.
- Stay ready for the next audit: Automatic audit trails and e-signatures aligned to 21 CFR Part 11 and EU Annex 11, with document and SOP control built in.
Specs, test results and lot release on the same record as the formulation, so a deviation traces back to its cause in minutes, not weeks.
Trusted by product and PLM leaders to keep the product record connected from first formulation through commercialization.
- One bill of materials, always current: BOMs stay structured, versioned, and connected to the formulation and raw-material records behind them, not a static file that drifts.
- See where every ingredient is used: Where-used shows every product a raw material touches, so a supply change or ingredient flag propagates instead of surprising you later.
- Know your margin as you develop: Unit costs roll up from the recipe to a cost per kilogram against target, so pricing decisions happen alongside formulation, not after it.
From approved formula to commercial product, with every BOM, version and change tied back to the lab data behind it.
Trusted by R&D and innovation leaders to see the whole portfolio, decide on evidence, and catch stalled projects and resource conflicts before they cost a quarter.
- See the whole portfolio in one view: Every project, stage, milestone, and resource in a single live dashboard, not a deck that is stale on arrival.
- Decide on evidence, not opinion: Each project links to its experiments, formulations, and QC results, so gate reviews are grounded in what actually happened in the lab.
- Catch stalled projects and resource conflicts early: Time-in-stage and resource load surface the projects that need attention before they cost a quarter.
Every project, stage gate and request in one view, with go/kill decisions backed by the experimental data, not status reports.
Compliance checked at the formula, not after it. Every ingredient links to a maintained regulations database, so formulations are screened against target markets while they're being designed.
- Screen as you formulate: Flag restricted or limited ingredients by jurisdiction before a sample is made.
- Re-check on change: When an ingredient or a regulation changes, see every affected formulation.
- One record from lab to label: Regulatory status travels with the formulation into PLM and quality, not into a separate file.
Compliance checked at the formula, not after it, with every ingredient screened against your target markets as you design.
Built for the materials you work with
From coatings to cell therapies, Uncountable models your ingredients, processes and tests as they are, configured to your industry.
Specialty Chemicals
Petrochemicals & energy
Adhesives & sealants
Lubricants
Surfactants
Pigments & dyes
Advanced Materials
Composites
Plastics, rubber & elastomers
Construction materials
Glass & ceramics
Pharma & Biotech
Biologics
Cell & gene therapy
Biomaterials
Medical devices
Food & Agriculture
Alternative proteins
Plant science
Crop protection
Flavors & ingredients Nutrition & supplements
Connected to the systems you already run
Uncountable sits at the center as the system of record for R&D and quality data, with a comprehensive API and integration layer connecting the systems around it.
Security, compliance and integrations
Uncountable meets the security and compliance bar enterprise product development requires, backed by independent third-party audits. Your data stays isolated per customer, encrypted in transit and at rest, and covered by a complete audit trail, with a 99.9% uptime SLA and a 10-minute RTO/RPO.
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Structure first, AI second
AI is only as good as the record beneath it. Uncountable structures every experiment, spec, lot and compliance check first, so Bodie reasons over real data, not loose files.
FAQs
The platform is the shared data layer. The five suites (Research & Development, Quality, Product Lifecycle, Regulatory Management and Project Management) are views into it, organized by the job to be done. You buy the platform and turn on the suites you need.
No. Teams commonly start with one suite, such as R&D or Quality, and add Product Lifecycle, Regulatory Management and Project Management over time. Every suite shares one data model, so expanding never means a new integration project.
It doesn't move, because there is one system. A formulation created in R&D carries its full context into regulatory checks, quality and PLM on the same record, and a change to one ingredient is traceable everywhere it's used.
Uncountable connects to lab instruments, bidirectional ERP integration, and data warehouses through a comprehensive REST API, webhooks, and bulk ingestion, with single sign-on. It acts as the central system of record for R&D and quality data.
Bring one real project. Watch it become one record.
