At Turnstone, we carry out internal audits specifically tailored to GDP (Good Distribution Practice) and medical device regulatory requirements. Whether you’re operating under EU GDP Guidelines, preparing for MHRA inspection, or maintaining your ISO 13485 quality system, our audits are designed to reflect real-world processes—not just tick boxes.

Led by experienced consultants and a qualified Responsible Person (RP), we assess how your current procedures, records, and controls align with industry-specific compliance requirements.

Our internal audits include:

• Full system audit against GDP requirements or ISO 13485 standards
• Review of your Quality Management System (QMS), SOPs, and documentation
• Checks on temperature control, traceability, complaints, and deviation handling
• Audit trails for product release, storage, transport, and cleanliness standards
• Actionable audit reports with non-conformances, risks, and recommendations
• Follow-up support with CAPA planning and staff training if required

We tailor each audit to your business, your product type, and your regulatory obligations—ensuring you’re fully prepared for external audits and inspections.

With Turnstone, you don’t just get an internal audit—you get expert insight and practical support to keep your system strong, compliant, and audit-ready every day.