The European market for monoclonal antibodies and related biopharmaceutical innovations is poised for significant growth as these therapies become central to treating complex diseases like cancer and autoimmune disorders. As antibody engineering technologies advance, there is an increasing need to optimize manufacturing processes, from scale-up to purification, to meet the growing demand for high-efficacy treatments. This event is crucial for the market as it addresses the critical challenges in antibody production, such as enhancing manufacturability, ensuring regulatory compliance, and improving yield and purity.
Antibody Engineering Europe 2025 will provide a comprehensive platform where experts and industry leaders can delve into the latest advancements in antibody engineering. With sessions focused on innovative manufacturing technologies, high-throughput screening, and downstream processing, the event will offer actionable insights into optimizing antibody production. Attendees will also explore cutting-edge topics like the implementation of single-use technologies, automation in biomanufacturing, and the integration of computational approaches for antibody optimization.
In addition to the technical sessions, the event will foster an intimate environment for one-on-one networking, allowing participants to forge meaningful connections that drive future collaborations. The conference is not just a gathering of industry professionals but a critical forum for shaping the future of antibody engineering in Europe. By addressing both current challenges and future opportunities, Antibody Engineering Europe 2025 is essential for anyone looking to stay at the forefront of biopharmaceutical innovation.
FEATURED CONTENT
Antibody Engineering Europe 2025
Agenda at a glance
Highlights of the Program
Why IMAPAC Event
Floor Plan
F.A.Q
Advances in Antibody Engineering for Enhanced Manufacturability
.
Process Development and Optimization
High Throughput Screening for Optimal Antibody Production
Strategies for Improving Yield and Purity
Scale-Up and Technology Transfer
Scaling Up from Lab to Pilot Plant
Technology Transfer: Best Practices and Case Studies
Implementing QbD (Quality by Design) in Antibody Manufacturing
.
Regulatory Considerations in Antibody Manufacturing
.
Manufacturing Technologies and Innovations
Single-Use Technologies in Antibody Production
Automation and Digitalization in Biomanufacturing
Computational Approaches in Antibody Optimization
Downstream Processing and Purification
Advances in Chromatography Techniques
Novel Purification Strategies for Complex Antibodies
Innovations in Antibody-Drug Conjugates (ADCs)
.
No data was found
No data was found
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 types 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 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 advantages does this conference offer to 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.
How can I register for the event?
To register for the event, please visit our registration page on our website. You’ll find detailed instructions and options for registration, including pricing and deadlines.
Can I submit a presentation or be a speaker at the event?
We welcome presentation submissions. If you’re interested in speaking at the event, please visit our “Call for Speakers” page on our website for submission guidelines and deadlines.
Are there sponsorship or exhibition opportunities available?
Yes, we offer sponsorship and exhibition opportunities for businesses and organizations. Please visit our “Sponsorship Opportunities” page on our website for more information.
What safety measures will be in place at the event to ensure the well-being 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.
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.
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.
Catch the limited super access in time to save BIG!
Local Biopharma/Academic
Limited Super
GBP850
*END-USER PRICING IS APPLICABLE to :
Company Profiles: Local Biopharma and BIG Pharma, Europe Academic & Research Institutes
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations.
Catch the limited super access in time to save BIG!
Local Biopharma/Academic
Limited Super
GBP850
*END-USER PRICING IS APPLICABLE to :
Company Profiles: Local Biopharma and BIG Pharma, Europe Academic & Research Institutes
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations.