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ADC Manufacturing Europe 2026
#ADCManEurope2026
WHERE EUROPE & ASIA MEET TO ACCELERATE THE NEXT GENERATION OF ADC PROCESS DEVELOPMENT & MANUFACTURING ALIGNMENT
Where cross-border leaders come together to define what successful ADC innovation and manufacture looks like in practice: from high-potency logistics to harmonised analytics and next-generation conjugation.
Dublin
28
October
-
29
October
2026
00
Days
00
Hours
00
Mins
00
Secs
+
Attendees
200
Maximum Attendees
100
+
Companies
60
+
Speakers
16
+
Networking Hours
+
Case Studies
Interactive Sessions
About the Event
Antibody-Drug Conjugates (ADCs) are among the most complex therapeutic modalities in biopharma and the technical, analytical, regulatory, and supply chain challenges that accompany them demand specialised solutions.
ADC Manufacturing Europe 2026 is where cross-border leaders come together to define what successful ADC innovation and manufacture looks like in practice: from high-potency logistics to harmonised analytics and next-generation conjugation.
Europe is rapidly building its ADC capabilities, but fragmentation in supply chains, inconsistent analytical standards, and the gap between Asian innovation and European manufacturing continue to slow progress. ADC Manufacturing Europe 2026 addresses these challenges head-on by bringing together senior technical, supply chain, and operational leaders responsible for delivering real-world ADC programmes, not just the science on paper.
This is not a generic scientific showcase. This is where operational and technical leadership meets strategic execution:
• De-risking high-potency payload (HPAPI) and linker logistics from Asia into Europe
• Accessing next-generation bispecific ADC (bsADC) designs and novel linker chemistries through co-development and licensing pathways
• Standardising analytical assays for seamless comparability and tech transfer across continents
• Scaling robust, compliant manufacturing and stability workflows with advanced analytics and predictive tools
Why Attend?
• Europe’s only forum dedicated to the operational and analytical realities of ADC manufacturing from procurement to GMP-ready deliverables
• Purpose-built for ADC decision-makers in Supply Chain, Conjugation Science, Analytical Development, Tech Ops, MSAT, CMC, and Quality
• Real-world case studies, interactive sessions, and benchmarking discussions that tackle fragmentation, variability, and execution risk
• Insights into multi-shore collaboration models that unlock innovation in conjugation and bispecific platforms at scale
If your role touches on getting complex ADCs from concept through conjugation into consistent, compliant manufacture, this is the room where those problems get solved.
Core Themes for 2026
Supply Chain Integration & HPAPI Logistics
Solving the “fragmentation fracture” in ADC supply chains by de-risking the movement of high-potency payloads and linker chemistries from Asian suppliers into European manufacturing environments.
Next-Gen Conjugation & Bispecific Innovation
Exploring access to Asian innovation in bispecific ADCs (bsADCs) and cutting-edge linker technologies, and shifting from traditional outsourcing toward co-development and licensing frameworks that accelerate pipeline progress.
Analytical Harmonisation & Tech Transfer
Standardising critical analytical assays (e.g., DAR, free payload quantitation, stability) to enable seamless technology transfer and product comparability between European development labs and Asian contract manufacturing partners.
Manufacturing, Stability, & Analytical Excellence
Practical frameworks and tools for scaling ADC production and ensuring product quality:
- Process Scale-Up & Continuous Processing: Retrofitting legacy facilities for perfusion and intensified workflows
- Advanced Characterisation: Aligning multi-modal analytics (MS, NGS, LC-MS) across borders
- AI-Driven Formulation & Predictive Stability: Using data models to anticipate and mitigate complex stability challenges
- Quality, Regulatory, & GMP Frameworks: Ensuring MHRA/EMA compliance across multi-shore development and manufacturing environments
Agenda at a Glance
View the Key Themes for
ADC Manufacturing Europe 2026
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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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*Delegate tickets must be purchased under the correct classification.
Biopharma tickets are strictly reserved for professionals employed by pharmaceutical or biopharmaceutical companies that develop, own, or commercialise therapeutic drug products, including organisations with an internal drug pipeline spanning discovery, development, clinical, or commercial stages. This category applies to companies whose primary business is the development or manufacture of drug products, not the provision of enabling technologies, equipment, platforms, or services.
Service, Solution, and Technology Provider tickets apply to all organisations offering services, platforms, technologies, equipment, consultancy, manufacturing services, or commercial solutions to the pharma and biopharma industry. This includes, but is not limited to, CROs, CDMOs, technology and equipment vendors, consultants, suppliers, and solution providers, regardless of scientific or technical focus.
Important Notice
All registrations are reviewed to ensure correct classification. Purchasing an incorrect ticket does not guarantee entry to the event. IMAPAC retains full discretion to deny access, reclassify registrations, and issue an invoice for the price difference required for correct attendance. Incorrect ticket purchases made under an inappropriate classification are not eligible for refunds under any circumstances, including where the registrant chooses not to upgrade or attend.
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Pre Conference Workshops & Other Sessions
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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 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.
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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