Industry

Biotech & Biopharma Procurement

Procurement tooling for biologics manufacturing, cell and gene therapy, and CDMO projects. Designed for teams sourcing process equipment in regulated environments.

Common challenges we help with

Bioreactor and single-use equipment sourcing is fragmented across emails and spreadsheets

Centralised RFQ workspace with all supplier responses, documents, and comparisons in one place.

Supplier qualification documentation for CDMO and biologics manufacturing is complex

Vendor document register organises certificates, test reports, and qualification evidence by supplier and document type.

Scale-up projects require tracking dozens of process equipment items simultaneously

Project-level procurement dashboard with equipment-level RFQ tracking and status visibility.

AI assistance raises questions in GxP environments

AI suggestions are labelled with model version and confidence. Human review and approval step before any AI result enters a regulated record.

Handover to the quality team at project close is unstructured

Deviation and document registers are structured for export. Full project handover ZIP is on the Phase 1 roadmap.

What is built for biopharma procurement today

These features are available now. This is not a claim of full GxP compliance.

  • Audit trail on all procurement events — attributable to named users with UTC timestamps
  • Regulated RFQ mode with process classification and risk tier fields
  • Vendor document register for biologics qualification documentation
  • AI governance controls — human-in-the-loop, model/version logging, confidence display
  • Tenant data isolation — no cross-company data sharing
  • GDPR data subject request management
  • Enterprise data isolation mode (ISOLATED) for sensitive biopharma projects
  • Data export available on request — you own your data

What is still being built

The following are on our roadmap: 21 CFR Part 11 e-signatures, formal validation documentation pack (IQ/OQ/PQ), ASME BPE and single-use equipment evidence fields, multi-step approval workflows, and certificate expiry alerts.