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
Finding qualified vendors for bioreactors, single-use systems, and other specialist biologics equipment quickly
AI supplier discovery searches the web and scores candidates against your sourcing brief with source-linked evidence, in minutes. Results are clearly marked as unverified and require team confirmation before any invitation is sent.
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. A human review and approval step is required 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.
- Find qualified vendors for specialist biologics and single-use equipment with AI sourcing and source-linked evidence
- 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 with model/version logging and confidence display
- Tenant data isolation, no cross-company data sharing
- Enterprise data isolation mode (ISOLATED) for sensitive biopharma projects
- Data export available on request, you own your data