Advancing Scalable, Compliant & Innovative Cell & Gene Therapy Production in the DACH Region

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Secure Early-Bird Pricing of £699 - Register Your Interest

AGENDA AT A GLANCE

DAY 1
DAY 2

Unlocking Commercial Success in DACH’s Cell & Gene Therapy

Quality Assurance in CGT
Industry Roundtables: What's Next for Bioprocessing in CGT?
Novel Purification & Intensification Strategies
Overcoming Bottlenecks in Viral Vector Manufacturing
Manufacturing Innovations for Allogeneic and In Vivo Therapies
Decentralized Production for Next-Gen Cell & Gene Therapies
Smart Factories: The Role of Digitalization & AI
Drink Reception
End of Conference

As the Cell & Gene Therapy (CGT) industry matures, the DACH region is emerging as a critical hub for commercial manufacturing and global supply.

Yet, the road from clinical promise to large-scale delivery remains paved with technical, regulatory, and supply chain challenges — particularly in viral vector capacity, closed-system adoption, and digital factory readiness.

CGT Manufacturing DACH 2026 will unite leaders from biopharma, biotech, CDMOs, regulators, and technology innovators to exchange practical solutions for scaling production, maintaining quality, and enabling global distribution.

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Key Themes & Topics

At the heart of CGT Manufacturing DACH, the programme addresses commercial scale-up, manufacturing innovation, and regulatory excellence in advanced therapies:

Industry Roundtables: The Future of CGT Bioprocessing

Interactive discussions with senior leaders on upcoming trends, regional opportunities, and global competitiveness in cell & gene therapy manufacturing.

Overcoming Bottlenecks in Viral Vector Production

Strategies to improve yields, streamline upstream and downstream processes, and manage facility constraints for scalable viral vector supply.

Quality Assurance & Regulatory Compliance in CGT

Addressing GMP, QC, and evolving regulatory requirements for both clinical-stage and commercial-scale manufacturing.

Novel Purification & Intensification Strategies

Exploring next-generation purification platforms, continuous processing, and intensified manufacturing for improved efficiency and throughput.

Manufacturing Innovations for Allogeneic & In Vivo Therapies

Adapting production systems for diverse therapy types, from donor-derived cell therapies to in vivo delivery platforms.

Smart Factories: Digitalization & AI in CGT

Leveraging Digital Twins, automation, and AI to enable predictive, data-driven manufacturing and faster process optimization.

200 max

Senior Attendees

Join the exclusive and focused gathering that unites the DACH region’s cell & gene therapy manufacturing leaders. Connect with senior decision-makers driving the scale-up, compliance, and commercialization of advanced therapies, from viral vector production to allogeneic and in vivo platforms.

30+

Expert Speakers

Gain first-hand insights from industry pioneers on overcoming manufacturing bottlenecks, optimizing closed and automated systems, intensifying production, and ensuring GMP compliance. Learn from real-world case studies shaping the future of CGT manufacturing in DACH and beyond.

20+

Companies Represented

Engage in targeted networking sessions to exchange expertise, discuss regulatory and operational challenges, and explore partnership opportunities with peers, CDMOs, and technology innovators in advanced therapies.

EXPECTED AUDIENCE SNAPSHOT

Attendance from

Biopharma

40%

Attendance from

Big Pharma

50%

Attendance from

Academia

10%

Decision Makers
0%

By Geography

BY PROFILE

0%

European Biopharma & Big Pharma

0%

International Biopharma & Big Pharma

0%

CDMO & CMO

0%

Technology & Service Providers

0%

Academic & Research Institutes

BY JOB TITLE

0%

C-Suite

0%

VP/Director

0%

Division Heads

0%

Senior Scientist

0%

Business Development

Target Attendee Snapshot

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Job Functions

Cell & Gene Therapy Manufacturing
Technical Operations
Bioprocessing (Upstream & Downstream)
MSAT (Manufacturing Science & Technology)
Process Development
Analytical Development
Quality Assurance & GMP Compliance
Regulatory Affairs (with ATMP/Gene Therapy focus)
Clinical Development & Translational Medicine
R&D – Biologics & Advanced Therapies
Supply Chain & Cold Chain Logistics
Technology Transfer
Business Development & Licensing
Strategic Partnerships & Corporate Development
CMC Development
Drug Product & Fill-Finish
Automation & Digital Manufacturing
Innovation & Platform Development

Seniority

C-Suite
Executive VP
Senior Vice President
Vice President
Director
Head of Department
Senior Manager
Team Lead / Functional Lead
Principal Scientist / Investigator
Qualified Person (QP)
View the 2025 Post-Event Report
View the Brochure

Bronwyn Westmore

Marketing Led

bronwyn.westmore@imapac.com

Farzana Begum

Operations & Marketing Executive

farzana.begum@imapac.com

Harry Liddiard

Project Manager

harry.liddiard@imapac.com