At Turnstone, we help you build robust, compliant supply chain documentation that supports full traceability, quality control, and regulatory compliance—especially within GDP and medical device supply chains.

Whether you’re working towards MHRA or ISO 13485 compliance, or simply tightening your oversight, we work with your team to design clear, practical documentation that reflects the reality of your supply chain operations.

Our support includes:

• Creation and review of Approved Supplier Lists
• Development of supplier quality agreements and documentation packs
• End-to-end traceability records from receipt to dispatch
• Procedures for supplier audits, delivery checks, and non-conformance management
• Integration of temperature monitoring and product handling protocols
• Support with documentation for outsourced services, including transport and storage

We ensure your supply chain documentation fits into your wider Quality Management System (QMS), helping you meet regulatory expectations and prepare confidently for external audits or inspections.

With Turnstone, your supply chain records do more than meet requirements—they become a reliable, working part of your compliance strategy.