Matrix Quality for Suppliers to Life Sciences

Component suppliers, contract manufacturers, and service providers to the life sciences industry must meet the quality system requirements of their customers and regulators. Matrix Quality helps you qualify, document, and demonstrate your quality standards at any time.

The challenge
Our solution

Common workflows

Quality processes for life sciences suppliers and contract manufacturers.

Document control and SOPsManage your quality system documentation with controlled review, approval, and version tracking — ready for customer audits and ISO 13485 certification.

  • Controlled document management

  • Version control with full change history

  • E-signatures and audit trail

CAPA and customer SCAR managementManage your own CAPAs and respond to customer supplier corrective action requests through a dedicated portal — all tracked, documented, and auditable.

  • Internal CAPA workflow

  • Customer SCAR portal access

  • Investigation and corrective action documentation

Audit readinessMaintain your quality system in a constant state of audit readiness. Training records, controlled documents, CAPA, and change control are all organised and retrievable on demand.

  • Customer and third-party audit management

  • Finding management and CAPA links

  • Audit evidence readily accessible

Training and competency managementTrack personnel training and competency against your quality system requirements — with a live training matrix to demonstrate qualification status to customers and auditors.

  • Role-based training assignment

  • Completion evidence and audit trail

  • Live training matrix for customer and auditor review

Hear from our customers

Roche

Matrix Quality gives us a single, validated system for our entire quality process. Audits that used to take weeks of preparation now take days.

Quality Director, Life Sciences Company

Matrix One is trusted by 500+ Life Sciences & Medical Device Companies