Smithers Medical Device Testing Division Passes MHRA & FDA Audits, Strengthening Quality and Testing

Smithers Medical Device Testing Division Passes MHRA & FDA Audits, Strengthening Quality and Testing

Smithers Medical Device Testing Division has successfully passed regulatory audits by both the Medicines and Healthcare products Regulatory Agency (MHRA) and the Food and Drug Administration (FDA), solidifying our commitment to quality in everything we do. Our quality management system (QMS) is harmonized across our global facilities ensuring consistent adherence to Good Manufacturing Practices (GMP) guidelines. 

These successful audits allow Smithers to continue to deliver results that support batch release testing of finished drug products. Our MHRA GMP certification, which verifies our commitment to GMP and quality management, is available when contacting an expert.

In addition to our continuous improvement and unwavering focus on quality, we offer seamless scalability as we expand our services, allowing testing for our customers to begin immediately and be delivered on time. 

Contact our experts to learn how Smithers can support your GMP testing needs. 
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