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QbD Group delivers multidisciplinary audits for Pharma, Biotech, and MedTech.

Keeping your operations compliant and audit-ready can be challenging, especially when juggling evolving regulations, supplier oversight, and maybe limited resources.

An audit helps you identify gaps, strengthen your QMS, and build lasting improvements across your organization.

QbD Group's certified auditors bring hands-on global experience across GxP, QMS (ISO), and regulatory frameworks. Whether you need support with a specific supplier/site assessment or your full annual audit plan, we combine compliance checks with actionable guidance to keep you inspection-ready.

We go beyond the audit, helping you understand findings, address them effectively, and prevent future issues. The result? Fewer surprises, stronger systems, reduced risk, and faster time to market.

Certified global GxP auditors

ISO, GMP, GDP, GCP & more

On-site or remote audits

Wherever you operate worldwide

End-to-end support

From planning to CAPA follow-up

Actionable insights, not just reports

Practical guidance you can act on

Why work with us

We perform a wide range of audits including GxP (GMP, GDP, GCP, GLP, GVP), ISO 13485, MDR & IVDR, QMS, supplier/vendor audits, mock inspections, and internal audits — across Pharma, Biotech, and MedTech.

Yes. We offer both on-site and remote audit capabilities. Remote audits follow the same rigorous methodology and deliver equally actionable findings, suitable for supplier assessments and document-heavy reviews.

We respond within 1 business day. Depending on scope and auditor availability, most audits can be scheduled within 2–4 weeks of initial contact.

Our certified auditors have deep expertise in pharmaceuticals, biotechnology, medical devices, IVDs, combination products, and companion diagnostics.

Absolutely. We go beyond the report — helping you understand findings, prioritize corrective actions, and implement CAPAs to build lasting compliance improvements.