GENEWIZ SNP/Mutation Analysis from Azenta Life Sciences is designed to follow Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP) as applicable to our services, and Good Clinical Practice (GCP) guidelines. Validate diagnostic assays with confidence and detect genetic mutations accurately, empowering you to achieve clinical success.
Azenta can sequence and analyze your clinical trial samples or confirm your diagnostic assay results according to FDA and EPA GLP standards. Simply provide SNP IDs, genes, or sequences of interest and Azenta can design, develop, and optimize your assays. Azenta’s experienced scientists and Quality Assurance Unit will ensure your assays are processed and reported according to the applicable regulatory standards.
Assay validation services for diagnostic kit and medical device 510k and PMA submissions are available at the GLP-compliant level.
For more information, please email regulatory@azenta.com.
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State-of-the-Art, Dedicated GLP Laboratories
Outsource to the Industry Leader in Sanger Sequencing
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Proprietary Protocols
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