At Turnstone, we help businesses build and maintain traceability systems that meet the strict requirements of Good Distribution Practice (GDP), pharmaceutical compliance, and ISO standards, such as ISO 13485. Our consultancy support ensures your traceability procedures, documentation, and training are clear, compliant, and easy to manage  giving you full visibility and control across every stage of your operation.

We understand that traceability isn’t just a paperwork exercise it’s a vital part of product integrity, audit readiness, and regulatory confidence. 

That’s why our team work closely with your team to design systems that work in practice, not just on paper.

Our traceability support includes:

• Development and review of traceability procedures to align with GDP, MHRA, and ISO requirements.

• Creation of compliant traceability forms, templates, and records that are simple to use and easy to audit.

• Design of recall, withdrawal, and incident response processes with clear roles, responsibilities, and documentation.

• Verification of supplier, storage, and transport traceability links to ensure end-to-end compliance.

• Training and awareness sessions to build understanding and consistency in record-keeping across your team.

• Ongoing support and system reviews to maintain accuracy, improve efficiency, and demonstrate continual compliance.

With Turnstone, you don’t just meet traceability requirements, you build a system that strengthens your compliance, protects your products, and supports your business reputation.

With Turnstone, traceability becomes more than record-keeping, it becomes proof of control, quality, and trust.