GXP-Storage eliminates the complexity and risk of fragmented regulated materials storage for life sciences organizations worldwide. Operating facilities in North Carolina's Research Triangle and Biomanufacturing Crescent region, and the UK's Golden Research Triangle region, we provide a unified, inspection-ready solution that consolidates your storage needs across the regulated product ecosystem, encompassing pre-clinical and clinical research, manufacturing, and healthcare. Our ISO-certified facilities, specialized equipment, quality management system, and validated GXP-Guardian platform ensure that you're always audit-ready, with restricted access, environmentally controlled storage, validated environmental monitoring, complete chain-of-custody documentation, visibility of materials in transit and at rest, and automated compliance reporting. We specialize in lifecycle management of a range of materials, including pre-clinical research materials, investigational medicinal products (IMPs), clinical trial samples, biologics and biosimilars, APIs and raw materials, stability and retention samples, reference standards, comparators, and environmentally-sensitive material that require secure preservation (from -150°C to controlled ambient conditions). With over 100 years of combined experience, our leadership team is trusted by biopharma, life sciences, and healthcare partners to deliver best practice solutions. We transform fragmented logistics and regulated storage from a compliance burden into a strategic advantage—reducing risk, ensuring data integrity, and keeping you inspection-ready at all times. Visit us online to learn more about how GXP-Storage protects your most valuable assets: www.gxp-storage.com