ISO 13485

Purchasing and Supplier Control Procedure

Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements.

Fully Customizable Audit Ready Instant Download
Standard
ISO 13485
Document Type
Procedure
Format
DOCX
Language
English
Tags
ISO 13485, Medical Devices, Procedure

This procedure defines how your organisation ensures that purchased product and outsourced processes conform to specified purchasing requirements, as required by ISO 13485:2016 clauses 7.4 and 4.1.5.

What's Inside

  • Supplier Classification
  • Supplier Evaluation and Selection
  • Approved Supplier List
  • Quality Agreements
  • Purchasing Information
  • Verification of Purchased Product
  • Supplier Monitoring and Re-evaluation
  • Non-Fulfilment of Purchasing Requirements

ISO 13485 Alignment

Supports ISO 13485:2016 requirements, including Clauses 4.1.5 and 7.4. It fits with the rest of the QEHS Vault ISO 13485 document set.

Format

Supplied as a fully editable Microsoft Word (.docx) file. Add your organisation’s name, logo and details, then use it straight away. Instant download after purchase.

Key Benefits

  • Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements