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ADC Manufacturing & Outsourcing 2026 focuses on the critical design, CMC, tech transfer, engineering, and outsourcing decisions that determine ADC manufacturability, regulatory flexibility, and long-term supply resilience.

The future of Antibody-Drug Conjugate manufacturing will not be decided at commercial scale.
It will be determined far earlier, in design decisions, CMC architecture, tech transfer strategy, engineering choices, and outsourcing models.
ADC Manufacturing & Outsourcing 2026 is the only dedicated forum focused on the critical pre-scale phases that define whether an ADC programme succeeds (or struggles) long before GMP execution begins.

ADC innovation is accelerating rapidly. Pipelines are advancing into clinical and commercial stages faster than ever before.
Yet across the industry, a pattern is emerging:
These are not production problems; they are design, transfer, and partnership problems.
ADC Manufacturing & Outsourcing focuses on the interfaces:
This is where long-term manufacturing success is shaped.
ADC manufacturing challenges do not sit within a single function. And they do not sit within a single organisation.
ADC Manufacturing & Outsourcing addresses ADC manufacturing as an integrated ecosystem, spanning innovator and CDMO environments.
Embedding manufacturability, lifecycle flexibility, and outsourcing readiness into early development.
Linker-payload strategy, conjugation architecture, and early CQA identification.
Building resilient CMC frameworks from early development through commercial readiness.
Comparability planning, lifecycle management, and regulatory alignment across internal and outsourced networks.
Selecting and structuring CDMO partnerships for potent ADC programmes.
Balancing control, flexibility, and speed.
Managing knowledge transfer, governance, and long-term collaboration models.
Governance frameworks that reduce friction between development and GMP sites.
Analytical and process transfer strategies that minimise variability and regulatory risk.
Facility design for high-potency payload handling.
Occupational exposure control and containment architecture.
Engineering solutions across conjugation, purification, and formulation.
Digital and PAT-enabled manufacturing concepts.
This is not a large-scale production conference. It does not focus on retrospective GMP success stories. Instead, ADC Manufacturing & Outsourcing concentrates on:
This event is the strategic complement to ADC Manufacturing Europe (Dublin, 28 - 29 October 2026), which focuses on manufacturing execution and operational scale.
The UK defines the strategy. Ireland delivers the scale.
The global ADC landscape is entering a decisive phase. Scientific innovation has accelerated dramatically. Manufacturing governance, CMC strategy, and outsourcing frameworks have not kept pace.
ADCs combine:
As programmes advance, the industry is increasingly encountering:
Most conferences focus on downstream GMP execution. The market lacks a dedicated forum addressing the earlier strategic decisions that determine manufacturability, comparability, and long-term supply reliability - across both innovator and CDMO environments.
ADC Manufacturing & Outsourcing fills that gap.
This conference is designed for senior and specialist professionals responsible for designing, transferring, and outsourcing ADC manufacturing programmes, including:
If your role influences how an ADC is designed, governed, engineered, or outsourced... this is your forum.
The UK is a global hub for:
London provides a natural meeting point for the decision-makers shaping ADC manufacturing pathways worldwide.
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ADC Manufacturing & Outsourcing 2026
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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.
Join the roster of esteemed colleagues to discuss what you or your company are bringing to the biopharmaceutical industry.
Apply to SpeakSelect the relevant ticket for your organisation.
*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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The conference will provide a comprehensive learning experience covering various aspects of the dynamic biopharmaceutical industry, ensuring attendees gain valuable insights and knowledge.
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.
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.
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.
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
Yes, we have networking sessions, workshops, and social events scheduled throughout the event to facilitate connections and collaborations among attendees.
Yes, we offer sponsorship and exhibition opportunities for businesses and organizations. Please visit our this page on our website for more information.
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