Security-first AI for pharma
- Hardware-encrypted AI inference. Auditors welcome.
- Purpose-built solutions for pharma manufacturing, designed against EU GMP Annex 11 and draft Annex 22
- Swiss-headquartered
Send your GxP data to AI without exposing it to plaintext — even during inference
When you send GxP data to GPT, Claude, Gemini, or Grok, it is processed in plaintext on the provider's infrastructure. For regulated pharma, that is a non-starter. ColdVault keeps your data encrypted end-to-end, including during inference itself — not a policy promise, a hardware guarantee. The open-source models we run on this infrastructure match leading proprietary models on independent public benchmarks and our own benchmark — open methodology and live results at benchmark.coldvault.ai.
Flagship products
Live and piloting today. Full portfolio at the bottom of every page.
Stage: LiveEncrypted AI inference infrastructure running leading open-source models inside hardware-attested AMD SEV-SNP confidential VMs. Customer-managed keys and per-request attestation your client verifies — so even we are architecturally unable to decrypt your data during inference. Models on this infrastructure match leading proprietary models on independent public benchmarks. Multi-model debate — models discuss, disagree, converge — measurably outperforms single-model baselines on real production tasks. Pinned model versions for validated workflows. Swiss-headquartered. The foundation every product on this page runs on.
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Stage: LiveAI-audited view of your manufacturing integration chain — ERP through middleware, MES, SCADA, and equipment, monitored as one continuous layer. Pharma teams run monitoring tools (Grafana, Datadog) for live operational visibility AND validation platforms (Veeva, Kneat) for GxP-signed system descriptions. The gap between them is filled today by human-produced PDFs that go stale the moment they're written. GlassHood bridges the two: generates the controlled, signed system-description artifact regulators require, from observed reality. Anchored to EU GMP Annex 11 §4.3 verbatim; we run it on our own infrastructure.
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Stage: LiveAI test execution that reads existing test documents and navigates UIs autonomously. Recorded-script test automation breaks when the UI changes — and pharma UIs change often. Test teams either rewrite scripts continuously or fall back to manual testing. TestRobin adapts as the UI changes, produces audit-ready evidence reports, and doesn't require testers to code. Mixed UI + API testing; designed against ALCOA+, Annex 11, and 21 CFR Part 11 electronic-evidence requirements.
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Stage: PilotingAI batch-record validation engine for regulated manufacturing. Batch review today relies on statistical sampling — typically 5% of records, manually checked. The other 95% are unreviewed; deviations hide there until they surface as recalls. BatchGuard reviews with full coverage and surfaces issues at review time for a qualified reviewer to act before they become formal deviations. Currently in active pilot with a global pharma manufacturer; designed against ALCOA+ and Annex 11 electronic-record requirements.
Learn more →Beyond the solutions above, 9robots is building domain-specific pharma LLMs (Scout, GxP, Flash, Heavy), operations and process- intelligence tools (OpsPulse, OperatorPartner, Hardware Robots), and automation (RunRobin, ColdVault Code) — across every stage from live to early research. See the full portfolio →
Don't take our word for it
Get a free API key with access to our encrypted open-source models. Rate-limited, minimal contract setup, no budget approval needed — enough for your technical team to verify the encryption and attestation claims first-hand.