Newsletter | October 17, 2025

10.17.25 -- Comparing Manual Vs. Automated Processing And Thawing Systems

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The 3rd Cell Therapy for Autoimmune Disease Summit (December 2-4, Philadelphia, PA) is your insider access pass to the latest cutting-edge data driving clinical progression across the autoimmune cell therapy. Immerse yourself in the future of autoimmune treatment with a revitalized agenda and an 80% new speaker panel, showcasing innovations translating clinical promise into meaningful patient outcomes. Find out more

FOCUS ON SUPPLY CHAIN

Comparing Manual Vs. Automated Processing And Thawing Systems

In this segment of our Cell & Gene Live, Optimizing Storage Solutions for iPSCs, expert panelists Pratik Jaluria, Ph.D., SVP Technical Development Strategy at BlueRock Therapeutics, Bruno Marques, Ph.D. VP, Process and Product Development at Century Therapeutics, and Kate Rochlin, Ph.D., COO at IN8bio share that a well-constructed manual operation can be matched by an automated system, but there is a higher capital expenditure.

Navigating Commercial Logistics: Key Considerations For CGT Manufacturers

A successful cell and gene therapy launch demands a comprehensive logistics strategy that keeps patients at the center, anticipates and mitigates disruptions, and proactively prepares for growth and global expansion.

SUPPLY CHAIN SOLUTIONS

GORE® STA-PURE® Flexible Freeze Container - W.L. Gore & Associates

FOCUS ON CLINICAL TRIALS

NK-Specific Strategies To Unlock Full Therapeutic Power

In this segment of Cell & Gene Live, Building the Future of Cancer Immunotherapy Through Allogeneic NK Cell Innovation, expert panelists Raphael Ognar, President, CEO, and Co-Founder of NKILT Therapeutics and Tracy Ryan, Co-Founder and Chief Communications Officer of NKore BioTherapeutics, emphasized that natural killer (NK) cells require distinct, tailored activation methods to unlock their full therapeutic potential in cancer. They argued that unfair comparisons with T cells hinder innovation and highlighted how NK-focused engineering boosts both persistence and cytotoxicity.

Enabling Investment In Community Hospitals To Improve Patient Access

Learn why enabling community hospitals to alleviate system constraints could catalyze a transformative shift in the future delivery of cell and gene therapies.

Four Pivotal Categories To Elevate Your Clinical Vendor Management

For sponsors ready to improve vendor management, technology platforms with the right framework can help you tighten budget controls, improve data integrity, or foster collaborative vendor relationships.

Why The Regional Site Manager Is The Swiss Army Knife Of Clinical Trials

The Regional Site Manager (RSM) monitoring model eliminates numerous clinical trial risks by leveraging efficient, start-to-finish site management by a single, expert point of contact.

Ocular Endpoint Protection In A Capital-Constrained Market

Ocular Endpoint Protection reframes data capture as a non-negotiable driver of efficiency, and sponsors who embed point-of-need (PON) into their protocols protect both their investment and results.

Navigating Adverse Immunostimulation: A Practical Guide For Clinical Researchers

Delve into how a systematic and scalable approach to evaluate adverse immunostimulation (AIS) in drug development through standardized biomarker sampling and tailored management strategies.

How Strategic Resourcing Accelerates Biotech's Path From Preclinical To FIH

Explore how strategic resourcing, particularly through FSP models, empowers biotech sponsors to overcome common hurdles transitioning when from preclinical research to first-in-human (FIH) trials.

Fomenting A Culture Of Analytical Excellence In Clinical Development

Building an "analytics culture" in clinical research requires striking a balance between fast, flexible technologies and the right support for trial teams working to integrate these solutions.

CLINICAL TRIALS SOLUTIONS

Connecting Highly Qualified Patients To Clinical Trials - Quest Diagnostics

Reviewing Protocols Across Therapeutic Areas - BRANY

EVENTS

Advancing the Future of Cell & Gene Therapy

This 11-12 November, Cell 2025 unites 1,000+ leading experts across the CGT value chain to solve key challenges, from scalable bioprocessing and regulatory hurdles to accelerating development timelines.

 

Gain practical strategies across cell culture, therapy development, and CGT manufacturing, and hear from world-renowned leaders Bobby Gaspar (CEO, Orchard Therapeutics), Christof Von Kalle, (Director & BIH Chair, Research Clinic Luxemburg), and Dame Molly Stevens (University of Oxford). Register Now

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