BBG Advanced Therapies collects first cell donation on one-of-a-kind bus

Progress When Systems Stand Still: Resilience and Access in Cell and Gene Therapy

Blueprint for Breakthroughs is a LinkedIn newsletter published by Adrienne B. Mendoza, MHA, SVP BioBridge Global and Chief Operating Officer (COO), BBG Advanced Therapies

Originally published on LinkedIn on October 7, 2025

This week, as the lights flicker in Washington and the nation feels the uncertainty of a government shutdown, the desert sun in Arizona seems to shine even brighter. At the Alliance for Regenerative Medicine’s Meeting on the Mesa, the cell and gene therapy community is alive with optimism, purpose, and momentum.

Inside the conference halls, the conversations are rich with possibility—how to accelerate clinical development, expand access, and build systems that can weather disruption. It’s a striking contrast: one part of our national infrastructure has slowed, while another is surging forward through collaboration and creativity.

That contrast is revealing. Progress in advanced therapies requires designing for resilience.

Resilience in Real Time

For those of us working in cell and gene therapy, moments like this remind us how interconnected science and systems truly are. The government shutdown is more than a policy event—it’s a stress test. It exposes where our infrastructure depends too heavily on stability and where it’s flexible enough to adapt.

And yet, progress continues. Across the country, research teams are still collecting cells, running assays, and analyzing data. Partnerships are forming. Trials are enrolling. Innovation moves forward not because the path is smooth, but because the people leading it refuse to stop.

That’s the defining strength of this field: its ability to turn disruption into determination.

Designing for Continuity and Connection

The regenerative medicine community has learned to build for resilience. From supply chains to regulatory frameworks, we’re learning to design continuity into the system—to ensure that therapies, trials, and patients are not left waiting when external pressures rise.

This spirit of adaptability is at the heart of what’s happening here at the Mesa. The connections being made this week represent more than professional alignment; they’re the foundation for shared problem-solving across an ecosystem that depends on partnership.

Progress in advanced therapies isn’t a solo effort—it’s a collective design project. One where data, infrastructure, and collaboration form the true scaffolding of innovation.

Access as the Engine of Progress

Resilience exists for a purpose: to create access that endures. Every innovation ultimately leads to a patient, and every system we design should be built with that patient in mind.

When systems stall—whether due to funding gaps, logistics, or geography—patients feel it first. That’s why access and scalability are not just operational priorities; they are the moral architecture of this field.

I often think of patient access and market scalability as the twin rails for progress—the structure that supports not only innovation, but the shared progress that turns science into solutions. Together, they create the space for the leap of faith every breakthrough requires: the courage to build systems that don’t yet exist, but must.

A Blueprint for What Comes Next

I’m honored to be speaking here on Wednesday morning here, about one such example of innovation—scaling access through a mobile model for leukapheresis. It’s a new approach to bringing regulated, high-quality cell collection directly to patients and communities, especially those historically underrepresented in clinical trials.

It’s one idea among many that share a common purpose: to ensure the future of cell and gene therapy is not only innovative, but inclusive and sustainable.

The government shutdown will pass. But the lesson it offers will stay with us. Progress doesn’t wait for perfect conditions—it depends on the systems we build, the people we trust, and the collective resilience we cultivate along the way.

When the lights flicker, the work continues. That’s the power of progress when systems stand still.

Article content

BBG Advanced Therapies and CELLforCURE Partner to Provide Transatlantic Manufacturing Solutions for Advanced Therapy Medicinal Products (ATMPs)

Collaboration establishes a transatlantic connection enabling U.S. companies to leverage CELLforCURE’s manufacturing capabilities in Europe, while European companies can benefit from BBG Advanced Therapies’ production capacities in the U.S

SAN ANTONIO, Texas — BBG Advanced Therapies, a subsidiary of BioBridge Global (San Antonio, Texas, USA), and CELLforCURE, part of SEQENS Group, (Les Ulis, France) are proud to announce a partnership dedicated to supporting the development and large-scale production of Advanced Therapy Medicinal Products (ATMPs).

This collaboration establishes a transatlantic connection enabling U.S. companies to leverage CELLforCURE’s manufacturing capabilities in Europe, while European companies can benefit from BBG Advanced Therapies’ production capacities in the United States. Together, they provide enhanced global CDMO capacity and an integrated service network to support the development and manufacturing needs of ATMP developers.

BBG Advanced Therapies integrates cell and tissue expertise with cutting-edge biomanufacturing capabilities, which include a strong track record in MSC-based projects as well as adherence to relevant FDA, EMA and PMDA regulations. Supporting innovators with progressing early-stage development through late-phase readiness and market launch, BBGAT’s holistic ecosystem of services spans leukapheresis, donor management, testing, cryopreservation and assay development, all under a unified Quality Management System. BBGAT has 9 cGMP cleanrooms spanning over 558 m2 (6,000 sq. ft.) and a process development space spanning over 232 m2 (2,500 sq.

ft.). With an eye toward advancing the industry and expanding patient access, BBGAT also maintains the world’s only mobile leukapheresis center.

CELLforCURE, EMA-authorized and FDA-compliant, combines a unique blend of CDMO heritage and proven commercial manufacturing expertise from Phase I to full-scale commercial production. Its “one-stop-shop” facility spans 10,000 m², including 3,000 m² (32,291 sq. ft.) of GMP-certified areas across 7 independent manufacturing lines, each with 8 cleanrooms, ensuring maximum safety and compliance for every product. CELLforCURE has a strong track record in CAR-T manufacturing as well as immune cells therapies, standing as a trusted, comprehensive solution provider. The company enables seamless project development by leveraging in-house Quality Control for 90% of processes, ensuring high-quality drug product delivery.

United by a shared vision to remove barriers in ATMPs manufacturing solutions, this collaboration creates a fully scalable, global CDMO partnership between USA and Europe that accelerates the journey from concept to commercialization. By combining transatlantic expertise and infrastructure, the partnership enables therapy developers to scale rapidly, launch multinational trials, and reach patients more effectively. Together, BBG Advanced Therapies and CELLforCURE now offer state-of-the-art GMP manufacturing space, providing unmatched capacity to support global clients.


About BBG Advanced Therapies: BBG Advanced Therapies provides innovative and custom solutions to accelerate the development of cell and gene therapies. BBG Advanced Therapies features a fully integrated and custom portfolio of innovative solutions, including collection and processing of starting materials, testing, clinical trials support, and biomanufacturing services. BBG Advanced Therapies is a subsidiary of BioBridge Global and is based in San Antonio, Texas. Learn more at BBGAdvancedTherapies.org.

About BioBridge Global: BioBridge Global is a 501(c)(3) nonprofit healthcare services enterprise headquartered in San Antonio, Texas, that offers diverse services through its nonprofit subsidiaries – South Texas Blood & Tissue, QualTex Laboratories, BBG Advanced Therapies and The Blood & Tissue Center Foundation. BioBridge Global provides products and services in blood resource management, cellular therapy, donated umbilical cord blood and human tissue, as well as testing of blood, plasma and tissue products for clients in the United States and worldwide.  The enterprise enables advances in the field of regenerative medicine and advanced therapies by providing access to starting materials, testing services, biomanufacturing and clinical trials support.  BioBridge Global is committed to saving and enhancing lives through the healing power of human cells and tissue.  Learn more at BioBridgeGlobal.org. 

About CELLforCURE: CELLforCURE SAS is a CDMO authorized by ANSM (French Regulatory Authority), dedicated to ATMPs production from concept to commercialization. With advanced technologies, extensive capabilities, and large-scale capacity, CELLforCURE offers a seamless journey from early-stage development to commercial manufacturing of a wide range of cell therapies. CELLforCURE is part of SEQENS group. Learn more at cellandgene.seqens.com.

About SEQENS: SEQENS is a global partner in health, personal care and specialty ingredients. We empower innovation to bring the best solutions to our customers, with a constant concern for sustainability. Relying on the skills of 3300 employees, we leverage a worldwide manufacturing network of 15 manufacturing sites and 9 state-of-the-art R&D centers in 9 countries. As an end-to-end player across the value chain, SEQENS offers a broad range of active ingredients, pharmaceutical intermediates, personal care & specialty ingredients. We innovate, develop and industrialize the most demanding molecules, and implement the best available technologies. Learn more at seqens.com.

BBG Advanced Therapies Logo Transparent
CellforCure logo