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Category: Cell & Gene Therapy


From Lab to Landmark: What Europe’s First Nonprofit Gene Therapy Approval Means for the CGT Community

Part 25 of our Bridging the Gap Series (Summary of the webinar session held in December 2025) Editor’s note: Since this webinar, Waskyra has also received approval from the U.S. Food and Drug Administration (FDA), expanding access beyond Europe. One of the hardest challenges in cell & gene therapy (CGT) is determining how programs for ultra-rare diseases […]

From Discovery to Delivery: Building Smarter Regulatory Pathways for Cell and Gene Therapy

Part 24 of our Bridging the Gap Series (Summary of the webinar session held in November 2025) Access to life-saving cell and gene therapies depends not only on scientific breakthroughs but also on the systems that bring those breakthroughs to patients. Regulations, infrastructure, and collaboration across borders determine whether a therapy moves from the lab to the […]

Connecting the Dots in Cell and Gene Therapy: The Power of Shared Purpose and Patient Hope

Part 23 of our Bridging the Gap Series (Summary of the webinar session held in October 2025) The last decade has seen a revolution in the way cell and gene therapies are developed, delivered, and accessed. What began as pioneering work in bone marrow transplantation has evolved into a global ecosystem advancing engineered cell therapies that offer […]

Decentralizing CAR-T in Europe: Inside and Beyond Hospital Clínic de Barcelona’s ARI Program

Part 22 of our Bridging the Gap Series (Summary of the webinar session held in September 2025) 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 […]

Optimizing Cell Viability in a GMP Workflow

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, […]

10 Reasons to Use Dry Thawing in Cell Therapy Processes

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 […]

Creating Accessible Cell and Gene Therapies — The World Can’t Wait

Part 21 of our Bridging the Gap Series (Summary of the webinar session held in August 2025) 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 […]

The Urgency of Now: Accelerating Access to Cell & Gene Therapies

Part 20 of our Bridging the Gap Series (Summary of the webinar session held in July 2025) 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 […]

The Goldilocks Goal in Long-Term Follow-Up for Cell & Gene Therapies: Finding the “Just Right” Approach

Part 19 of our Bridging the Gap Series (Summary of the webinar session held in June 2025) 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 […]

5 Ways Optimized Cell Line Management Helps Streamline Cell Therapy Workflows

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 […]