A regulated-grade platform where brands, formulations, batches and audits coexist — without compromising on the tenancy boundaries that the industry demands.
Products, BOMs, suppliers, plants, packaging. One schema, soft-deleted, versioned, exportable.
Product Development Profiles linked to bills of materials. Every component traceable to a supplier and a lot.
Onboard suppliers via a structured portal. Lead times, MOQs, certifications and documents — all in one place.
Component, WIP and finished goods inventory tracked by lot, with expiry, quarantine and release states.
Demand-driven purchase orders, blanket agreements, supplier scorecards, dual-sourcing rules.
OEE-adjacent metrics for CDMOs: on-time release, scrap rate, lead-time drift, supplier compliance.
Live bridges to SAP, Oracle, Microsoft Dynamics and major MES platforms. Bidirectional, idempotent, observable.
Every write is recorded with actor, tenant, timestamp and old/new value. 21 CFR Part 11 evidence on demand.
Multi-level BOMs versioned per brand and per regulatory market. Substitution rules, allergen flags, regional restrictions — surfaced at planning time, not after the batch is poured.
Certifications expire. MOQs change. Lead times drift. IRIS Procurement tracks the contract, the document, the score — and refuses to schedule a run against a supplier whose paperwork has lapsed.
Every write is logged with actor, tenant, IP, old value, new value. Soft-delete preserves history forever. Exports tailored to FDA 21 CFR Part 11, EU GMP Annex 11, MHRA, ANSM.
A German CDMO produces for 14 cosmetic brands and 4 pharma clients on the same site. Each tenant has its own BOMs, suppliers, scheduling rules — and never sees the others.
When a brand reformulates a serum, the new BOM is versioned, the impacted suppliers re-qualified, the schedule re-planned. The auditor arriving next month will see every change, with timestamps, signatures and reason codes.
The plant manager doesn't think about compliance any more. IRIS Procurement is the compliance.
If you operate under GMP, the demo includes a Part 11 walk-through. We bring the auditor questions; you bring the data.