FAQ / Biopharma & Research
Biopharma & Research
Information for pharmaceutical and research partners on companion diagnostics, clinical studies, and biomarker discovery services.
Partnership, clinical trials, and data collaboration
FAQs for Biopharma Partners
Yes. We have 30+ clinical projects to date and offer end-to-end genomics support for clinical trials, including sample processing, bioinformatics analysis, variant reporting, and data management. Contact us at support@codexgenetics.com to discuss your project.
Yes. Our bioinformatics team can design custom gene panels tailored to your trial endpoints and biomarker hypotheses. We can also provide pharmacogenomics (PGx) profiling for patient stratification.
We can deliver results in standard formats including VCF, BAM/FASTQ, and curated variant tables. We also offer structured clinical reports in PDF and HL7 FHIR-compatible formats on request.
Yes, subject to import/export regulations. We have experience coordinating international sample logistics. Please contact us to discuss your study's geographic scope.
We are ISO 27001 certified. All data is processed under our Data Processing Agreement (DPA), which is available on request and complies with Hong Kong PDPO requirements.
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Hong Kong-based molecular diagnostics laboratory specialising in clinical genomics, precision oncology, and rare disease diagnosis. Accredited to ISO 27001 and GenQA standards.
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