Built On
Veridata OS gives early-stage biotech and diagnostics companies production-grade execution infrastructure: compliance, lineage, workflow orchestration, so you can ship regulated products without building the plumbing.
Building an LDT or pursuing a CDx? Run your assay validation pipeline on compliant infrastructure from day one: variant classification, evidence generation, and regulatory lineage included.
Your model is only as good as the execution layer beneath it. Ship with deterministic provenance and full audit trails, not retrofitted compliance bolted on before your first FDA conversation.
Cohort discovery, site performance scoring, adaptive trial design, on infrastructure designed for 21 CFR Part 11 compliance. Cut months off your compliance timeline.
Batch tracking, chain of custody, release criteria, manufacturing execution: the workflow layer you'd otherwise spend a year building from scratch.
Run on Veridata's execution substrate with canonical data models, lineage, and auditability built in. No rewrites when you hit your first enterprise customer. No retrofitted compliance before your first audit.
Inherit validated execution logic for data provenance, reproducibility, drift control, and 21 CFR Part 11 workflows. You build the product value. Veridata handles the rules.
Selected partners receive credits-based platform access, joint reference architectures, enterprise introductions, and regulator-ready credibility. We help serious products reach regulated buyers faster.
We review your product, stage, and technical needs. The program is selective. We work with teams solving real problems in regulated healthcare.
Credits-based platform access, shared reference architectures, and hands-on technical onboarding. Deploy your application directly on the execution layer.
Co-selling into enterprise accounts, joint case studies, and introductions to regulated buyers as the program matures. Your traction compounds on infrastructure that's already trusted.