Carlsbad, California
BioReliance® Viral and Gene Therapy Manufacturing

We are a market leading CDMO that offers full range of manufacturing, product development, sterile fill finish and testing services. Our facility completed both a U.S. Food & Drug Administration (FDA) Pre-License inspection and a European Medicines Agency (EMA) Marketing Authorization inspection  We support scale-up, process validation, clinical trials and commercial launch. Our main manufacturing area features 16 client-dedicated Class 10000 (ISO 7) clean room production suites with single-pass cleanroom airflow systems exhausted directly from each clean room and two dedicated Class 1000 (ISO 6) fill suites.