Depend on GENEWIZ^TM Preclinical & Clinical Services from Azenta to support your preclinical and clinical regulatory submissions. Our state-of-the-art US Laboratory adheres to Good Manufacturing Practices (GMP), as applicable to our services, Good Clinical Practice (GCP) guidelines and is compliant with FDA and EPA Good Laboratory Practices (GLP) and accredited by the College of American Pathologists (CAP)/Clinical Laboratory Improvement Amendments (CLIA).

We offer a complete solution to support all your clinical and regulatory needs. From sample collection and storage, through to sample processing, sequencing, analysis, and reporting. Operating with the highest-quality standards, our flexible services are customized to meet each customer’s unique specifications.