From production to bedside: A tiered QC framework for regulatory alignment and analytical comparability in decentralized CGT

Decentralized and point-of-care (PoC) manufacturing is reshaping cell and gene therapy (CGT) by bringing production closer to patients. This model offers advantages, including reduced vein-to-vein times, streamlined logistics, and greater flexibility for patient-specific treatments, with the potential to improve affordability and broaden access. However, it introduces new quality control (QC) challenges that are central to ensuring product safety, potency, and consistency. Autologous CGTs, typically produced as single patient lots with limited shelf lives and compressed release timelines, require QC systems capable of delivering reliable results within hours for critical quality attributes (CQA) such as identity, potency, sterility, and safety. In both autologous and allogeneic settings, variability in starting material, shortages of trained personnel, and a lack of standardized assays across sites complicate consistency and hinder data pooling in multicenter trials. Hospital-based facilities also require enhanced infrastructure, harmonized procedures, and digital oversight to sustain network-wide comparability. Emerging solutions emphasize automation, validated rapid-testing platforms, and methods that minimize reliance on highly specialized expertise to accelerate batch release and improve reproducibility across distributed networks. Regulatory agencies are updating frameworks for modular and Point-of-Care (PoC) models, emphasizing flexibility while maintaining rigorous standards. Here, we outline a tiered QC model designed to maintain product comparability and enable timely release. QC has become the defining challenge of decentralized CGT manufacturing. However, implementing robust strategies, assay harmonization, and validated rapid-release methods can ensure uniform product quality across distributed sites, so that every patient, regardless of treatment site, receives safe, effective, and timely therapy.

Authors

Institutions

Publication Details

Journal
Regenerative Therapy
Published
2026-04-21
DOI
https://doi.org/10.1016/j.reth.2026.101112
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

From production to bedside: A tiered QC framework for regulatory alignment and analytical comparability in decentralized CGT

Devanshi Doshi, Emiko Jeffries, Kristine Nishida, Heiko von der Leyen et al.
Regenerative Therapy
CAR-T cell therapy research
article

From production to bedside: A tiered QC framework for regulatory alignment and analytical comparability in decentralized CGT

Devanshi Doshi, Emiko Jeffries, Kristine Nishida, Heiko von der Leyen, Vered Caplan, Sagi Nahum, Cris Kosnik
article en

Abstract

Decentralized and point-of-care (PoC) manufacturing is reshaping cell and gene therapy (CGT) by bringing production closer to patients. This model offers advantages, including reduced vein-to-vein times, streamlined logistics, and greater flexibility for patient-specific treatments, with the potential to improve affordability and broaden access. However, it introduces new quality control (QC) challenges that are central to ensuring product safety, potency, and consistency. Autologous CGTs, typically produced as single patient lots with limited shelf lives and compressed release timelines, require QC systems capable of delivering reliable results within hours for critical quality attributes (CQA) such as identity, potency, sterility, and safety. In both autologous and allogeneic settings, variability in starting material, shortages of trained personnel, and a lack of standardized assays across sites complicate consistency and hinder data pooling in multicenter trials. Hospital-based facilities also require enhanced infrastructure, harmonized procedures, and digital oversight to sustain network-wide comparability. Emerging solutions emphasize automation, validated rapid-testing platforms, and methods that minimize reliance on highly specialized expertise to accelerate batch release and improve reproducibility across distributed networks. Regulatory agencies are updating frameworks for modular and Point-of-Care (PoC) models, emphasizing flexibility while maintaining rigorous standards. Here, we outline a tiered QC model designed to maintain product comparability and enable timely release. QC has become the defining challenge of decentralized CGT manufacturing. However, implementing robust strategies, assay harmonization, and validated rapid-release methods can ensure uniform product quality across distributed sites, so that every patient, regardless of treatment site, receives safe, effective, and timely therapy.

Regenerative TherapyVol. 32
Intelligent Fusion Technology (United States) (US), Senseonics (United States) (US)
Industry, innovation and infrastructure
Openalex Percentile: Top 19%
CAR-T cell therapy research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.