Newsletter | May 5, 2026

05.05.26 -- Mapping Candel Therapeutics' Sprint To The BLA Finish Line

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Webinar: Cleanroom ISO Classification: The Framework for Containment in a Cleanroom

Explore how ISO classification shapes cleanroom design and GMP outcomes in advanced therapies. This webinar covers cell and gene therapy, viral vectors, mRNA, and sterile manufacturing, highlighting impacts on HVAC, pressurization, and containment strategy. Learn how early alignment of process and regulatory requirements prevents redesigns, reduces risk, and strengthens compliance. Insights show integrated planning enables scalable, inspection-ready ATMP facilities. Click here to learn more.

FOCUS ON MANUFACTURING

Mapping Candel Therapeutics' Sprint To The BLA Finish Line

Leaders from the adenovirus/prodrug developer discuss the complex balancing act of preparing to scale up for commercial manufacturing without overextension.

A Step-By-Step Guide To Cell Banking

Cell banking stands at the forefront of medical advancement. This guide delves into the steps involved in protecting these priceless resources, from cell collection and processing to storage and cell expansion.

How To Select The Right Platform For Your Vaccine Production Process

Evaluate surface treatments, scalability, and contamination risks to select the right adherent platform. Testing early ensures a seamless transition from benchtop to production.

Automated Library Prep For Nanopore Human Whole Genome Sequencing

Streamline long-read library preparation with an automated high-input workflow. Learn how to maintain large DNA fragments while significantly reducing reagent consumption for large-scale genomic projects.

Optimizing Transposon Delivery For Efficient CAR T-Cell Manufacturing

Discover how scalable electroporation enhances T-cell engineering. This method achieves high viability and yield when using transposon systems, facilitating more efficient manufacturing workflows.

How To Choose The Appropriate Filter Material For Every Sample

Membrane compatibility plays a crucial role in reliable sample filtration. Knowing how different filter materials interact helps prevent common workflow issues and supports efficient filtration.

Streamlining Cell Line Development For Antibodies

Accelerate antibody production from clone selection to commercialization. A robust strategy utilizing automation and advanced analytics helps streamline development and ensures clinical success.

The Most Exciting Frontiers In Cell Therapy Development

From high-dimensional profiling to customizable Omic panels, new technologies are redefining cell therapy development—delivering better insights, efficiency, and scalability for researchers worldwide.

Scaling Viral Vector Production Using Fixed-Bed Bioreactor Systems

Simplify the transition from development to manufacturing with fixed-bed bioreactors. Bridge consistent performance and simplified scale-up for your adherent recombinant viral vector processes. 

8 Key Steps To Reduce Contamination During Material Transfer

Implement this material transfer workflow to safeguard your cleanroom. Focus on barrier integrity, meticulous wiping, and surface preparation to reduce contamination risks.

Stability Of Supplemented PRIME-XV T Cell CDM At Room Temperature

Review data on supplemented medium stability for up to 72 hours at room temperature. Findings show consistent T cell expansion, viability, and marker expression for flexible manufacturing schedules.

MANUFACTURING SOLUTIONS

On-Demand Media And Buffer Manufacturing System - Nucleus Biologics

Innovations In Sterile Connectors Transform CGT Bioprocessing - CPC

CHO System That Supports Diverse Molecule Types - Asimov

Labeling For Form, Fill, And Seal Machines - HERMA

Accurate Single-Use Bag Filling System For Small Volumes - Single Use Support

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