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10901 Kenwood Road, Blue Ash, OH, 45242, US
Resilience is a North American CDMO focused on delivering high-quality, scalable manufacturing solutions for advanced therapies. With capabilities spanning biologics drug substance, cell-based therapies, and aseptic drug product manufacturing for both small and large molecules, Resilience partners with biopharma companies to bring complex medicines to market faster and more reliably. The company is building a streamlined, high-performance network designed to meet the evolving needs of clinical and commercial-stage innovators. For more information, visit https://resilience.com/ and follow us on social media: Resilience on LinkedIn.
How today’s manufacturers are filling the growing need for biologics without rushing complex processes in development or quality control.
By: Kristin Brooks
Advantages of integrated, QbD-guided formulation development services and key strategies for minimizing risk and maximizing success.
By: Eliza Yeung
As trade policy, regulatory scrutiny, and capital discipline reshape biologics development, sponsors are rethinking where and how commercial manufacturing is secured. Bora Biologics’ recent U.S. expansion and validated 2,000L scale-up reflect a broader shift toward demand-aligned, inspection-ready commercial capacity in the markets where products will ultimately be supplied.
Released By Bora Biologics
Epicrispr’s investigational gene therapy, EPI-321, is a treatment for facioscapulohumeral muscular dystrophy.
By: Patrick Lavery
The companies will use Cellular Origins’ automated mobile robotic platform.
The partnership will work to advance Novelty Nobility’s bispecific antibody drug candidate through process development and GMP manufacturing.
Expands its capabilities in next-generation biologics with Cizutamig, Candid’s lead investigational asset.
By: Charlie Sternberg
Expansions at sites in both the United States and Europe are crucial to PCI’s vision for the coming years.
Released By PCI Pharma Services
Plans for GMP release for production by the end of 2026.
To create US-APAC manufacturing corridor, enabling local production for global clinical trials.
Marks the sixth consecutive year that WuXi Biologics has received this honor
The designation certifies WuXi’s fitness for commercial manufacturing and quality management of drug-device combination products.
Will leverage Regeneron’s biologics expertise and Telix’s radiopharmaceutical development platform.
The partnership allows the Butantan Institute to expand its portfolio of advanced therapies.
It is the first such certificate issued to a 20,000-liter scale biologics facility in China.
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