germany-logo1
22th -
23th
October 2024 | 
Marriott Munich Airport Alois-Steinecker-Straße 20, 85354 Freising, Germany

ADVANCING BIOLOGICS R&D, MANUFACTURING, TECHNOLOGY & INNOVATION IN GERMANY

22th -
23th
October 2024 | 
Marriott Munich Airport Alois-Steinecker-Straße 20, 85354 Freising, Germany
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Germany's biopharmaceutical market has witnessed remarkable growth in recent years driven by significant advancements in the major European pharmaceutical market and ranked the fourth largest worldwide. These include increased investments in R&D, the expansion of biotechnology infrastructure and capacity, and a supportive regulatory environment. The German biologics market is projected to continue its upward trajectory, driven by rising demand for innovative biologic therapies across therapeutic areas such as oncology, autoimmune diseases, and rare disorders. In addition to local industry players like Bayer and Boehringer Ingelheim, many international pharmaceutical companies – including, for instance, GlaxoSmithKline, Pfizer, Roche, Sanofi and Takeda – operate production facilities in Germany.

The Biologics World Germany 2024 Conference stands as a premier gathering of biopharmaceutical professionals, with the primary goal of fostering collaboration, innovation, and knowledge exchange within the dynamic landscape of biologics R&D and manufacturing. Specifically focusing on Germany's burgeoning biopharmaceutical sector, this conference serves as a catalyst for bringing together key stakeholders, thought leaders, and industry experts to explore the latest advancements and challenges shaping the future of biologics development and production.

At the Biologics World Germany 2024, key topics such as best practices in biologics R&D, clinical research & trials, advancements in bioprocess upstream optimization and technology innovations, downstream processing cost-cutting strategies, continuous manufacturing and single-use systems, regulatory considerations, quality & analytics as well as commercialization strategies will be highlighted to address the evolving landscape of biopharmaceutical R&D and manufacturing. By bringing together industry leaders, researchers, and stakeholders, this conference aims to accelerate advancements in biologics development, production, and commercialization, further strengthening Germany's position as a global leader in the biopharmaceutical arena.

FEATURED CONTENT

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Biologics Manufacturing Germany 2024
  • Latest Innovations in Cell Culture Technologies
  • High-Throughput Screening for Cell Line Development
  • Next-Generation Bioreactor Systems
  • Cost- reduction strategies in recovery and purification of biologic drugs
  • Reducing Downstream Scale-Up Needs: Advances Toward Continuous Downstream Processing
  • Aseptic Considerations in Fill-Finish: Barrier vs. Isolator Tech
  • Advanced Analytical Techniques for Biophysical Characterization within Regulatory Frameworks
  • Analytical Tools to Improve Decision-Making During Product Development
  • Process Validation: Determining Required Process Performance Qualification Runs
  • Understanding Genome Editing for Cell-Line Development
  • Optimizing Biomanufacturing Processes with Industry 5.0 Innovations
  • Platform Optimization for Efficient AAV Purification
  • Is biomanufacturing a synergy of CDMOs, logistics, automation and AI?
  • Addressing the Key Pitfalls Hindering Technology Transfer Success
  • Key Aspects of Contamination Control Strategy in Vaccine and Biologics Production
  • Current and Emerging Technologies to Optimize mRNA Manufacturing
  • Enhancing Lyophilization Cycle Times and Stability for Complex Injectable Drugs
  • Addressing the Biopharma Talent Shortage
  • Navigating Disruptions: Building Resilience in Biomanufacturing Supply Chain Management
  • Role of Data analytics towards Industry 4.0.
  • Monitoring of fermentation processes by imaging and image analysis
  • Using AI  to replicate continuous manufacturing for advanced modalities
  • Strengthening vaccine Manufacturing: Collaborative Efforts for Localized Solutions – Ken Wong, Critical Material Management Lead (US Sites), Sanofi USA
  • Meeting the manufacturing challenge: To buy or build?
  • Optimizing Bioprocess Design: Integrating Facilities, Expertise, and Workflow Efficiency
  • Efficient cold chain management for advanced therapy trials
  • Unlocking the Complexity of Temperature-Controlled Packaging in the Supply Chain
  • Challenges in Developing Pre-Filled Packaging for Precision Dosing: Beyond Traditional Glass
  • Simplify, Derisk, and Accelerate ADC Development and Manufacturing Timelines
  • Advancements in Predictive Toxicology: Enhancing Predictive Capability with Novel Methodologies
  • Eliminating the Analytical Bottleneck in Production and Purification of mRNA

THANK YOU TO OUR SUPPORTING PARTNERS









SPEAKERS

Featuring esteemed voices from the biopharmaceutical sector. Our selected experts will share insights on the latest trends, challenges, and developments in this dynamic field. Engage in unique discussions, learn about cutting-edge scientific discoveries, and explore the future of biopharmaceuticals with these influential thought leaders. Don't miss this chance to broaden your understanding of this ever-evolving industry.

Barbara-Hartl_photo_profile

Barbara Härtl

Associate Vice President, Manufacturing Operations

Calidi Biotherapeutics
Germany
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Cornelia Thieme

Global Head of Pharmaceutical Science, Manufacturing Science & Technology

Galderma
Switzerland
David Vikstrome

David Vikstrom

CTO

Xbrane Biopharma
Sweden
no-picture

Elizabeth Oladipo

Quality Assurance Specialist

Abbott
Dublin
Florence Salmon

Florence Salmon

VP Reg Affairs

HOOKIPA Pharma
Austria
Jonggu-Kim_photo_profile

Jonggu Kim

External Manufacturing Large Molecules Gen Med & Vaccines Quality Leader,

Sanofi
South Korea
Ken-Wong_photo_profile

Ken Wong

Critical Material Management Lead (US Sites)

Sanofi
USA
Mohamed-Noor

Mohamed Noor

Digitalization Manager - Biopharma 4.0

NIBRT National Institute for Bioprocessing Research and Training
Ireland
image (3)

Tyler Goodwin

Head of Delivery and Process Development

Tune Therapeutics
USA

DELEGATE REGISTRATION

Catch the limited super access in time to save BIG!

END-USERS

Limited Super (By 17 May 2024)

GBP 850 

Limited Special (By 19 July 2024)

GBP 1,050

Early Bird (By 20 September 2024)

GBP 1,250

Standard Price

GBP 1,450

Service/Solution Providers

Limited Super (By 17 May 2024)

GBP 2,050

Limited Special (By 19 July 2024)

GBP 2,250

Early Bird (By 20 September 2024)

GBP 2,450 

Standard Price

GBP 2,650 

FEATURED CONTENT

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