Customer stories
Proof, not promises.
Real quality teams catching real signals — before they ever became a batch failure.
The QualityIntelligence Layerfor Pharma.
We ingest all your scattered data to catch quality failures before they happen.
The platform
Every Record.
Every System.
One Source of Truth.
Your data already holds the answers — scattered across systems, spreadsheets, and paper. Veriqa connects and validates every record into one source of truth: the documents you must produce, and the intelligence you've never been able to see.
Every source flows in
Veriqa links & validates every record
Answers flow out, audit-ready
Records & docs
Paper records
Quality events
Deviations
Systems of record
QMS data
Trends & data
Batch trends
Veriqa
validating · live
Use cases
How it works
From scattered records to a living quality brain.
Connect
Living brain
Audit-ready
By modality
Built for how you
actually manufacture.
One quality layer across every modality — APIs, oral solid dose, sterile injectables, and the CDMOs that make them.
API
Oral Solid Dose
Sterile
CDMOs
The impact
Faster releases. Fewer surprises.
Always ready.
One connected view of your quality data so releases move faster, problems surface sooner, and you're never scrambling before an inspection.
Directional outcomes — modeled against your own baselines during pilot.
In their words
We caught a cross-product yield drift weeks before it would have reached a batch record — something our spreadsheets could never surface.
Mid-size API manufacturer
Security & compliance roadmap
Architected for the world’s most demanding standards
Designed for
SOC 2 Type II21 CFR Part 11GAMP 5EU GMP Annex 11ICH Q10ISO 27001
Security specifications
EncryptionAES-256 · TLS 1.3
Access controlRBAC · SSO/SAML
Audit trailsImmutable · user-attributed
Disaster recoveryRPO < 1 hr · RTO < 4 hrs
FAQ
Questions,
answered.
Straight answers on compliance, validation, and what it takes to get Veriqa running on your stack.
Talk to our team →It can’t. Every figure traces back to its source record with proof, and the calculations are deterministic — same data in, same result out, not generative guesswork. Nothing enters a report until a qualified reviewer signs off.
Never used to train models (ours or anyone’s) and never shared across customers. Raw records are processed on our own infrastructure; any AI reasoning runs under zero-data-retention enterprise terms. Everything’s encrypted, access scoped by site and role, hosted in the region you require and your data is yours to export anytime.
Always. Veriqa surfaces the analysis — your team approves it, section by section, before anything advances. Nothing is finalized without a person signing off.
Inspectors review the document, not the tool. You hand them a human-signed APQR where every data point traces to its source, backed by a full audit trail. Veriqa handles the assembly and analysis; a qualified person owns and approves the final report.
No. Veriqa sits on top of the systems you already run. Nothing gets ripped out or migrated. All deployments start read-only, so nothing in your validated environment changes on day one.
Typically 2-3 days, not the 6–12 months a traditional QMS rollout takes. No on-site install, no new software to learn — your team logs in through the browser and starts. We load your historical data up front, so it’s useful from day one.
Still have a question?Talk to our team →