Beyond CAR-T: Building manufacturing strategies for the next generation of regenerative cell therapies

Webinar Date: September 10, 2026

Time: 11:00 AM EDT

Duration: 1 hour

As cell and gene therapy shifts toward in vivo approaches and regenerative modalities — iPSCs, MSCs, HSCs, and beyond — sponsors face new challenges beyond traditional CAR-T manufacturing: bioreactor and culture system selection, analytical strategy, and potency assay development for cell types with far less manufacturing precedent. Add to that the complexity of scaling from 2D to 3D culture systems, cryopreservation strategies for increasingly complex formats, and navigating regulatory pathways that are still being defined for these emerging modalities, and technical development can quickly become a bottleneck. This webinar will cover how Kincell Bio is expanding its platform to support these next-generation programs, including practical considerations for bioreactor selection, analytical and potency assay development, and regulatory strategy for early-stage sponsors. Attendees will leave with a clearer framework for planning technical development and manufacturing readiness.

In this webinar you’ll learn:

Engage early with your CDMO to de-risk technical development timelines
Select bioreactor and culture systems suited to your specific cell type and scale
Prioritize analytical and potency assay development based on regulatory risk, not convenience
Build cryopreservation and viability strategy into process design from day one
Anticipate regulatory expectations for emerging modalities before they become blockers

Who should attend:

Process development scientists
CMC/regulatory affairs specialists
Program/project leads at emerging cell therapy companies
Technical operations and manufacturing strategy leads

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