Pulse™: Cell line development from design to GMP master cell bank

Driving faster, clinically aligned iPSC cell line development with clean IP.

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Setting the standard in cell line development.

Pulse™ enables cell therapy innovators to simplify and accelerate the journey from iPSC line to GMP Master Cell Bank — uniting cell line design, reprogramming, gene editing, and GMP master cell banking (MCB) under one integrated platform with transparent, proprietary IP.

Drug Developer Pain Point Cellistic Solution
Speed & Safety

Traditional editing approaches can add up to 6 months per edit to development and increase risks to genomic integrity.

Cut 12+ months of your timeline

Checkmark IconSTAR-CRISPR™ multiplexing enables up to 4 gene edits in a single shot

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Automated high-throughput clonal selection with C.Station & UP.Sight

Clear IP Positioning

Licensing complexity and unclear IP hinder path to commercialization.

Integrated IP and licensing 

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All IP - including STAR-CRISPR™ and unedited and edited Allo Chassis™ lines-under one roof 

Regulatory Readiness

Advancing with confidence in a comparatively new regulatory environment.

Regulatory-ready from day one

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Rigorous QC/QA with low-passage banking ensures genomic stability, reproducibility, and monoclonality

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GMP Master Cell Banks, produced in an EMA-certified, FDA/PMDA-compliant facility

True End-to-End Continuity

Fragmented handoff between Cell Line Development and Manufacturing lead to rework, lost time, and added risk.

End-to-end continuity

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Seamless integration to GMP manufacturing of cell therapy drug product through our Echo™ platform

What Pulse™ delivers.

Cut timelines by 12+ months with iPSC cell line deliverables optimized for clinical readiness and manufacturing continuity — here’s what that includes:

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Fully characterized, GMP-compliant iPSC master cell bank

≥200 vials (≥1M cells each), low-passage and genomically stable.

Comprehensive documentation package 

Certificates of Analysis, Certificate of Compliance, traceability logs, clone histories, batch records.

Pre-validated release assays and QC panel 

streamlined handover to GMP manufacturing facility.

Manufactured in EMA-certified, FDA/PMDA-compliant facility 

backed by 15+ years of iPSC and GMP manufacturing experience and 100% program success rate.

IP under one roof 

direct access to STAR-CRISPR™ and Allo Chassis™ iPSC cell lines without third-party licensing

multi-vials

GMP master cell banking

Our turnkey process includes pre-qualified materials, rigorous quality control, genetic stability assessments, and comprehensive GMP documentation, providing the critical proof for your IND.

Pulse™: The integrated workflow for clinical-grade iPSCs.

Integrating scientific precision with operational scalability — and flexible enough to meet you at any stage of development.

STAR-CRISPR™ multiplex editing

Up to four simultaneous edits with high efficiency and minimal off-targets.

Automated clonal handling

C.Station & UP.Sight enable high-throughput screening for monoclonality, traceability, and optimal clone selection.

GMP-aligned process

Pre-qualified assays, defined materials, and standardized documentation eliminate R&D-to-GMP rework.

All IP under one roof

All core technologies — STAR-CRISPR™, Allo Chassis™, and GMP workflows — fully owned and licensed by Cellistic.

Off-the-shelf iPSC cell lines & GMP master cell banks.

Non-edited

Origin Gene Editing GMP MCB
CD34+ T-Cell - GMP MCB
CD4+ T-Cell - -

 

Allo Chassis™ (Edited)

Origin Gene Editing GMP MCB
CD34+ T-Cell
Double KO
(MHC-I/II null)
GMP MCB

CD4+ T-Cell Double KO
(MHC-I/II null)
GMP MCB

 

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Why Cellistic?

GMP manufacturing excellence

EMA-certified, FDA/PMDA-compliant GMP facility in Mont-Saint-Guibert (Belgium) combining industrialized processes and automation for consistent, clinical-grade manufacturing.

Enabling technologies

Proprietary platforms — Pulse™ and Echo™, technologies STAR-CRISPR™ and Allo Chassis™ — combined with end-to-end CDMO services to accelerate allogeneic iPSC-derived therapy development.

15 years of iPSC expertise

With over 15 years of focused iPSC innovation, our scientists have refined differentiation, scale-up, and analytical strategies that define industry benchmarks for consistency, potency, and quality.

Quality & reliability

Rigorous QC/QA systems and advanced analytical methods ensure consistent, compliant, and high-performing cell therapy materials.



Frequently asked questions

 

Not finding what you’re looking for? Contact us.

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Tune our platforms and technologies to your exact needs.

The next steps are clear: You learn more about our platforms and technologies (and the experienced team behind them). We talk about your immune oncology or regenerative medicine’s specific challenges and opportunities. And then together, we chart the ideal  path to advance your program to commercial success.