Access to advanced therapies is often framed as a challenge of resources and infrastructure. But in Europe, a bold new model is reshaping how patients receive life-saving CAR T-cell therapy. Instead of relying solely on commercial manufacturing and centralized approval processes, the Hospital Clínic de Barcelona has pioneered a hospital-based pathway that delivers CAR-T directly […]
View Blog
Cell and gene therapy (CGT) manufacturing can be complex. Part of the process requires precise, contamination-free thawing across a variety of critical materials. While we often focus on thawing cryopreserved cell products, another key component in CGT workflows is the controlled thawing of viral vectors used in gene modification. Researchers of King’s College London, UK, […]
View Blog
During cell therapy process development and manufacturing, you need unwavering trust in the technologies that you use. Barkey offers multiple solutions that deliver trust in the form of precise, gentle, yet robust dry thawing for your vials, bags, and bottles. Below are 10 great reasons to incorporate a Barkey dry thawing system. 10 Reasons to […]
View Blog
Providing access to transformative cell and gene therapies is one of the most urgent challenges in modern healthcare. These treatments offer the possibility of curing conditions once thought untreatable—yet in the United States, only a fraction of eligible patients are receiving them. The barriers are complex: financial risk for payers, short-term budgeting in a long-term […]
View Blog
Access to life-saving cell and gene therapies is one of the most critical challenges facing healthcare today. While these therapies offer remarkable hope for patients battling life-threatening conditions like cancer and rare genetic diseases, the reality is that only a fraction of eligible patients are actually receiving them. The reasons are rarely scientific. More often, […]
View Blog
In the rapidly advancing world of cell and gene therapy, a single treatment can alter a patient’s life trajectory. But what happens after the initial success? For many, the journey is just beginning. Long-term follow-up (LTFU) is not just a regulatory requirement—it’s a vital, ethical commitment to patients who become pioneers of new treatments. Yet, […]
View Blog
In the rapidly evolving field of cell therapy research, cell lines are a stable and renewable resource for investigating disease mechanisms, testing therapeutic candidates, and pioneering new cell-based treatments. Proper and efficient management of cell line data, license agreement terms, and audit logs are critical for success. Finding the right cell line management solution, like […]
View Blog
Access to advanced therapies that can fundamentally alter disease trajectories is one of the most pressing frontiers in healthcare. Among them, cell and gene therapies offer unprecedented hope for millions, especially those grappling with rare, chronic, or previously untreatable conditions. Yet, realizing the full potential of these therapies requires more than scientific innovation—it demands cross-sector […]
View Blog
Across the globe, access to life-saving cell and gene therapies like CAR T-cell therapy remains largely limited to wealthier nations and well-resourced health systems. While the clinical outcomes of these therapies can be extraordinary—offering cures for certain blood cancers—their high cost and complexity of production present a barrier that many countries cannot overcome. But a […]
View Blog
Mesenchymal stem cells (MSCs) have long shown promise in regenerative medicine, with the potential to treat everything from heart disease to autoimmune conditions. But for decades, MSC therapies struggled to move beyond early-phase clinical trials and regional approvals. That changed in December 2024 when the U.S. Food and Drug Administration (FDA) approved RYONCIL—and it became […]
View Blog