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PharmaXcelerate USA 2026 Biopharma Manufacturing, Scale-Up & Commercial Readiness

When it will happen
15 - 16 SEP 2026 / 08:30 - 16:30
Where it will happen
Philadelphia, USA
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PharmaXcelerate USA 2026 Biopharma Manufacturing, Scale-Up & Commercial Readiness

When it will happen
15-16 SEP 2026 / 08:30 - 16:30
Where it will happen
Philadelphia, USA
See Related Events
Click Here!
Days
Hours
Minutes
Seconds
Expired
65 +
Users
5 +
Sponsors
20 +
Speakers

ABOUT THE CONFERENCE

PharmaXcelerate USA 2026 brings together senior manufacturing leaders, engineers, and decision-makers from the biopharma and biotech industries to address one central challenge: how to successfully scale complex therapies into commercial reality. Taking place on 15–16 September 2026 in Philadelphia, this edition focuses on manufacturing scale-up, facility strategy, and operational readiness.

Across two days, delegates will engage with experts from leading organizations including AstraZeneca, Pfizer, Biogen, Moderna, Takeda, CSL Behring, and Eli Lilly, alongside engineering, quality, and manufacturing leaders shaping the future of biopharma production. The agenda is built around real-world case studies and operational insights, covering critical topics such as multi-modality facility design, Annex 1 compliance and contamination control, scaling biologics and advanced therapies, MS&T transformation, and the integration of AI, digital twins, and data-driven manufacturing systems. 

The program is designed to go beyond theory, focusing on what actually determines success at scale. Sessions explore how manufacturers are overcoming bottlenecks in tech transfer, managing multi-site and CMO networks, implementing predictive manufacturing through PAT and data science, and transitioning from reactive compliance to adaptive quality systems.

PharmaXcelerate USA is a focused, senior-level forum for professionals responsible for manufacturing strategy, facility design, process development, and operational performance. Join your peers in Philadelphia to exchange lessons learned, benchmark approaches, and explore the strategies and technologies defining the future of biopharma manufacturing in the US.

PRICING

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End User (1-2 Delegates)
€2,199.00
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End User (3-4 Delegates)
€1,999.00
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End User (5+Delegates)
€1,799.00
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Vendor Delegate
€2,499.00
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TOPICS AT A GLANCE:

  1. Global Biopharma Facility Design for Multi-Modality Manufacturing
  2. Sustainable Facilities: Annex 1, Energy & Long-Term Performance
  3. Aligning HSE, Engineering & Manufacturing at Scale
  4. AI Reshaping Biopharma Quality & Manufacturing
  5. Predictive Manufacturing via Digital Twin Integration
  6. PAT & Data Science Pipelines for Real-Time Intelligence
  7. Global CMC Expectations for mRNA & Advanced Therapies
  8. Risk & Science-Based Commissioning & Qualification
  9. Rethinking Quality Frameworks for Advanced Therapies
  10. Scaling Biologics from Clinical to Commercial Production

SPEAKERS

Edita Botonjic Sehic

Head of Process Analytical Technology & Data Science

Recipharm Advanced Bio

Norman Goldschmidt

Board Member

ISPE

Veera Padmanabhan

Executive Director, Head of Manufacturing Sciences and Technology

AstraZeneca

Aaron Larsen

Chief Scientific Officer,

Quill Therapeutics

Sai Prathyusha Bhamidipati

Director, Reg CMC

Moderna

Hazem Eleskandarani

Senior Director, Global Quality Engineering

CSL Behring

Nick Haycocks

Senior Specialist Quality Assurance

RoNiK

Kim Gauthier

VP, Head of Global Engineering and Facilities

Biogen

Gisèle Fahmi

Director, Acquisitions Collaborations and Divestitures

Pfizer

Mihaela Carmen Simianu

President and Principal Consultant

CONCORDIA MCS

Edwin Harmon

Senior Director, Engineering and Facilities

Eli Lilly

Arjun Channi

Senior Director, Global Regulatory Lead

Takeda

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Fouad Atouf

Chief Science Officer

US Pharmacopeia