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Biologics Manufacturing Germany 2025
#BMG2025
Germany's Premier Gathering for the Biopharma Community
Biologics Manufacturing Germany 2025 unites industry leaders to explore innovations and challenges in Europe's fourth-largest biopharma manufacturing sector.
Marriott Munich Airport, Germany
18
-
19
February 2025
00
Days
00
Hours
00
Mins
00
Secs
200
+
Attendees
100
+
Companies
30
+
Speakers
20
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Networking Hours
8
+
Case Studies
About the Event
Germany's biopharmaceutical sector ranks fourth globally with 650+ biotech companies, driven by strong industry-research-government collaboration and bioregions.
The sector experiences 8% annual prescription growth due to increasing chronic diseases and an aging population, with companies like Calidi Biotherapeutics, Eleva Biologics, and Roche benefiting from Germany's strategic advantages. #BMG2025, dedicated to propelling bioprocessing innovation and market expansion, will address these developments.
Featuring industry leaders like Uwe Gottschalk, event chairman, and representatives from Sanofi, Abbvie, and Roche, while offering 120+ networking opportunities and expert sessions on bioprocessing, CMC strategy, and facility design, focusing on critical issues such as risk mitigation, regulatory compliance, automation, AI, and sustainability in the evolving biologics manufacturing landscape.
What to Anticipate this Year?
📌 Engaging Thought Leadership from Uwe Gottschalk, leading as Event Chair, and over 30 hand-picked expert
speakers, providing curated insights and niche industry knowledge
📌 Big Pharma Presentation from Sanofi, Abbvie, Roche, Abbott, and more
📌 120+ Networking Opportunities with key stakeholders in the German biomanufacturing space, including
drinks receptions and targeted informal gathering
📌 Global Technological Showcase with an international exhibition of the latest biopharmaceutical technologies and services
📌 Expert-led sessions on bioprocessing, CMC strategy, and facility design. Implement continuous bioprocessing
with advanced analytics, modular design, and sustainable practices for optimized, eco-friendly manufacturing
Agenda at a Glance
View the Key Themes for
Biologics Manufacturing Germany 2025
Biomanufacturing in Focus: Advancing Efficiency, Collaboration, and Leadership in Germany
- Keynote Address: Building a Biomanufacturing Powerhouse: Synergies and Opportunities in Germany
- Turning Setbacks into Success: Conducting Effective Investigations in Manufacturing
- Turning Setbacks into Success: Conducting Effective Investigations in Manufacturing
- Panel: Biopharma Optimization Showdown: Intensify or Go Continuous?
Advances in Upstream Processing and Cell-Line Development
- Utilizing automation and AI to maintain optimal conditions for high-density culture
- Advanced High-Throughput Screening Solutions for Streamlined Upstream Processing
- High-Throughput Screening Strategies for Streamlined Cell Line Development
Downstream Processing Optimization
- Reducing Downstream Scale-Up Needs: Advances Toward Continuous Downstream Processing (CDSP)
- Enhancing Downstream Processing with Continuous Downstream Processing (CDSP) Solutions
- Tackling the challenges of antibody-drug conjugate (ADC) manufacturing: innovative purification techniques and process simplification strategies.
Optimizing Biopharmaceutical Quality: QbD, GMP, and Issue Resolution
- QbD: Architecting a Robust Manufacturing Future for Biopharmaceuticals
- GMP Requirements for Cell and Gene Therapy Manufacturing
- Effective CGT Issue Resolution: Root Cause Analysis and CAPA Management
- Case Study: Xbrane and the development of high quality Biosimilars
10 Round Table
- AI and Lab Automation for Biomanufacturing
- Addressing the Biopharma Talent Shortage
- Understanding Genome Editing for Cell-Line Development
- Optimizing Biomanufacturing Processes with Industry 5.0 Innovations
- Platform Optimization for Efficient AAV Purification
- 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
Harnessing the Power of AI and Big Data in Bioprocessing 4.0
- Industrial IoT (IIoT) Platforms for Decentralized Production and Smart Factories
- Industrial Platforms for Decentralized Production and Smart Factories
- Role of Data analytics towards Industry 4.0
Facility Design & CMC Strategies
- Integrate facility design and CMC considerations into the Biopharma Optimization Showdown.
- Key Ingredients for a Powerful CMC Strategy
- Panel: Key Ingredients for a Powerful CMC Strategy
Advanced Strategies in Tech-Transfer: Cost Management and Sustainable Practices
- Strategies to Mitigate Early Adoption Costs of GMP-Grade Materials
- Sustainable Strategies for Streamlining Tech-Transfer Processes in Biomanufacturing
- Examining sustainability in CMO selection: How to integrate it without compromising quality and cost competitiveness?
New Drug Modalities
- Manufacturing of Novel off-the-shelf allogeneic Virotherapies
- Panel: Manufacturing and Commercialization Process / Cost Optimization
Ready to attend?
Register today to secure your ticket.
Speakers
Esteemed Voices From the Industry
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.
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Daniel Heinzelmann
Process Expert in Cell Line Development
Boehringer Ingelheim
Germany
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Uwe Gottschalk
Operating Partner
Keensight Capital
Paris
Jason Beckwith
Professor
University of Dundee
United Kingdom
Vitaly Biniyaminov
Automation Expert
Steinbeis-Beratungszentrum Digitale Transformation und Prozessautomatisierung
Germany
Stephen Sullivan
COO
iPSirius
United Kingdom
Paul Matejtschuk
Head Formulation Science
Medicines & Healthcare Products Regulatory Agency
United Kingdom
Mohamed Noor
Digitalization Manager - Biopharma 4.0
NIBRT National Institute for Bioprocessing Research and Training
Ireland
John Manneke
Senior Procurement Manager/ Global Category Manager DS
Roche
Switzerland
Jan Talts
COO
Amniotics
Sweden
Ingo Gorr
Head of Therapeutic Virus Development
Boehringer Ingelheim
Germany
Harald Bradl
Director & Head of Downstream Development
Boehringer Ingelheim
Germany
Filippo Ramondelli
Associate Director CMC Lead
Takeda
Italy
Dr. Pavan Narayanaswamy
Head of CMC and Regulatory Affairs
AATec Medical
Germany
David Vikstrom
CTO
Xbrane Biopharma
Sweden
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Dainties Guzaukas
Senior CMC/ Regulatory Manager
InflaRx
Germany
Baerbel Grossmann
Associate Director Global Regulatory Affairs CMC Biologics
Sanofi
Germany
Andreas Schaaf
Managing Director/CSO
Eleva Biologics
Germany
Alexander Russell
Associate Director - Technical Operations
Abbvie
Ireland
Leopold Bertea
Chief Technology Officer
Mendus AB
Netherlands
Registration
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£2895 (+VAT)
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Join the roster of esteemed colleagues to discuss what you or your company are bringing to the biopharmaceutical industry.
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Exhibition & Networking
Wuxi Biologics
WuXi Biologics is a leading contract research, development and manufacturing organization (CRDMO) that provides end-to-end capabilities to healthcare organizations worldwide. With operations in China, the United States, Ireland, Germany, and Singapore, we enable our partners to effectively and efficiently bring biologics and vaccines to patients worldwide through our comprehensive and high-quality drug development model.
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Intelsius
We have been designing and manufacturing environmentally sustainable and regulatory compliant sample transport and temperature-controlled packaging for 25 years. Patient safety is always at the forefront of our product development. Ensuring your pharmaceutical products and biological samples arrive at their destination with their integrity intact is paramount. As well as offering a diverse range of sample transport and temperature-controlled packaging solutions, our expert Technical Services team and ISTA-certified laboratory ensure we can design, test and qualify your packaging with your specific payload and shipping lane in mind.
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Programme & Showcase
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Just Evotec Biologics
Just – Evotec Biologics, a wholly owned subsidiary of Evotec SE, is a technology-driven CDMO with locations in the USA and Europe. We provide our partners with highly differentiated services for the development and manufacturing of mAbs as well as next-generation biologics such as bi-specific/multi-specific antibodies and Fc fusion proteins, with experience extending to both NBE’s and biosimilar products. Our world-leading AI-driven in silico molecular optimization and continuous bioprocessing platforms combined with our revolutionary J.POD® facilities, which represent a paradigm shift within the industry, are helping to reduce the cost of goods and expand global access to affordable, high-quality biotherapeutics in addition to providing a highly agile cGMP manufacturing strategy to support rapid ramp up and uncertain demand scenarios.
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Coriolis Pharma
Coriolis Pharma is a global contract research and development organization (CRDO) and the premier partner for the development of liquid and lyophilized drug products, analytical services, and manufacturing services across a vast array of therapeutic modalities, including biologics, gene and cell therapies and vaccines. Our expert scientists design and execute platform and custom services under R&D and GMP to accelerate and derisk our clients’ programs right from the start and throughout the entire product lifecycle. Founded in 2008, Coriolis Pharma has established a global presence with offices in the EU and the US.
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ProBio
ProBio, a subsidiary of GenScript Biotech Corporation, offers end-to-end CDMO services from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in CGT, antibody and recombinant protein drug, aiming to accelerate drug development for customers. ProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 90 IND approvals since October 2017.
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Media & Publicity
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Pre Conference Workshops
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Co-Located Events
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Frequently Asked Questions
How can I stay updated on event details and announcements?
To stay informed about event updates, including date, venue, and agenda, please subscribe to our newsletter on our event website. You can also follow our official social media channels for real-time updates and announcements.
What can I expect to learn and explore during the event?
The conference will provide a comprehensive learning experience covering various aspects of the dynamic biopharmaceutical industry, ensuring attendees gain valuable insights and knowledge.
What safety measures will be in place to ensure the safety of attendees?
We are committed to ensuring the safety and well-being of all attendees. We will implement rigorous safety measures in line with local health guidelines and regulations. Specific safety measures will be communicated closer to the event date to ensure they align with the most up-to-date health recommendations. Rest assured, your safety is our priority.
Is there a cancellation or refund policy if I can't attend after registering?
Yes, we have a cancellation and refund policy in place. Please refer to our “Cancellation Policy” on our website for details on how to request a refund if you are unable to attend.
Can I submit a presentation to be a speaker at this event?
We welcome presentation submissions. If you’re interested in speaking at the event, please visit this page on our website for submission guidelines and deadlines.
What type of professionals benefit most from attending?
Our event is designed to cater to a wide range of professionals within the biopharmaceutical industry, including researchers, scientists, executives, regulatory experts, and professionals involved in drug development and manufacturing.
What advantages does this conference offer participants?
Participants can expect to gain insights from industry experts, network with peers, and stay up-to-date with the latest trends and innovations in biopharmaceuticals
Are there networking opportunities or special events planned?
Yes, we have networking sessions, workshops, and social events scheduled throughout the event to facilitate connections and collaborations among attendees.
Are there sponsorship opportunities for this event?
Yes, we offer sponsorship and exhibition opportunities for businesses and organizations. Please visit our this page on our website for more information.
How can I register for the event?
To register for the event, you'll find multiple "register" buttons on this page to get started. You’ll find detailed instructions and options for registration, including pricing and deadlines.
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