ADC Manufacturing & Outsourcing 2026
#ADCMan2026

WHERE ADC MANUFACTURING IS DESIGNED, CONTROLLED, TRANSFERRED - & STRETEGICALLY OUTSOURCED - BEFORE IT IS SCALED

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.

London
11
June
-
12
June
2026
00
Days
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Hours
00
Mins
00
Secs
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Attendees

150

Maximum Attendees

100
+

Companies

30
+

Speakers

16
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Networking Hours

+

Case Studies

Interactive Sessions

About the Event

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:

  • Scientifically strong ADCs prove operationally fragile
  • CMC strategies lack lifecycle resilience
  • Tech transfers expose analytical and knowledge gaps
  • Outsourcing relationships are structured too late - or too transactionally
  • Engineering constraints surface under pressure.

These are not production problems; they are design, transfer, and partnership problems.

ADC Manufacturing & Outsourcing focuses on the interfaces:

  • Where discovery meets development
  • Where CMC strategy meets regulatory expectation
  • Where innovators select and align with CDMO partners
  • Where development programmes transition into GMP environments
  • Where engineering decisions define scalability and containment

This is where long-term manufacturing success is shaped.

Why Design, CMC, Tech Transfer, Engineering & Outsourcing Together?

ADC manufacturing challenges do not sit within a single function. And they do not sit within a single organisation.

  • Design decisions affect manufacturability and partner selection
  • CMC strategy determines regulatory flexibility across sites
  • Outsourcing models shape knowledge retention and risk distribution
  • Tech transfer exposes gaps between development intent and GMP execution
  • Engineering determines whether processes are safe, scalable, and repeatable

ADC Manufacturing & Outsourcing addresses ADC manufacturing as an integrated ecosystem, spanning innovator and CDMO environments.

Core Themes for 2026:

Designing ADCs for Manufacturability & Transfer

Embedding manufacturability, lifecycle flexibility, and outsourcing readiness into early development.
Linker-payload strategy, conjugation architecture, and early CQA identification.

CMC Strategy & Regulatory Architecture

Building resilient CMC frameworks from early development through commercial readiness.
Comparability planning, lifecycle management, and regulatory alignment across internal and outsourced networks.

Strategic Outsourcing & CDMO Alignment

Selecting and structuring CDMO partnerships for potent ADC programmes.
Balancing control, flexibility, and speed.
Managing knowledge transfer, governance, and long-term collaboration models.

Right-First-Time Tech Transfer

Governance frameworks that reduce friction between development and GMP sites.
Analytical and process transfer strategies that minimise variability and regulatory risk.

Engineering & Containment Strategy for Potent Modalities

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.

What Makes #ADCMan2026 Different?

This is not a large-scale production conference. It does not focus on retrospective GMP success stories. Instead, ADC Manufacturing & Outsourcing concentrates on:

  • Decision-making before GMP execution
  • Translational challenges between development and manufacturing
  • Cross-functional alignment between science, regulation, engineering, and outsourcing partners
  • Designing manufacturing and outsourcing strategies that scale successfully

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.

Why Does the Market Need this Event?

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:

  • Biologics
  • Highly-potent small molecules
  • Advanced conjugation chemistry
  • Sophisticated analytics
  • Strict safety and engineering requirements

As programmes advance, the industry is increasingly encountering:

  • ADCs that are innovative but difficult to scale
  • CMC strategies that limit regulatory flexibility
  • Outsourcing models that expose knowledge gaps
  • Tech transfers that reveal analytical inconsistencies
  • Engineering misalignment discovered too late

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.

Who Should Attend?

This conference is designed for senior and specialist professionals responsible for designing, transferring, and outsourcing ADC manufacturing programmes, including:

  • CMC & MSAT leaders
  • Process and analytical development scientists
  • Tech transfer and manufacturing strategy leads
  • Regulatory affairs and quality strategists
  • Engineering and facility design experts
  • Strategic outsourcing and alliance management leads
  • Innovator biotech and advanced CDMO teams

If your role influences how an ADC is designed, governed, engineered, or outsourced... this is your forum.

Why London, UK?

The UK is a global hub for:

  • ADC discovery and translational science
  • CMC and regulatory strategy leadership
  • Engineering and containment innovation
  • CDMO and partnership ecosystems supporting potent modalities

London provides a natural meeting point for the decision-makers shaping ADC manufacturing pathways worldwide.

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Agenda  at a Glance

View the Key Themes for

ADC Manufacturing & Outsourcing 2026

Day 1 | 11 June 2026
  • Advances in ADC Payload & Linker Chemistry Scalable ADC Manufacturing Workflows
  • Payload Toxicity Management During CMC Development
  • ADC CDMO Case Studies & Showcase
  • Roundtable Sessions: Key Challenges of ADC Manufacturing Today and How to Get it Right First Time
Day 2 | 12 June 2026
  • Improving ADC Stability & Product Quality
  • ADC Supply Chain Design for CMC
  • ADC Case Studies: Why ADC’s fail?
  • Closing Panel Discussion: The ADC Playbook: Five Decisions That Matter Most

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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Want to Speak at This Event?

Join the roster of esteemed colleagues to discuss what you or your company are bringing to the biopharmaceutical industry.

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Registration

Select 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.

BIOPHARMA
Starting from £699 (+VAT)

Priority Access

Discounts automatically applied at checkout to secure preferrential rates

*Standard ticket pricing is £899+VAT. From 01 June 2026, standard pricing will apply

£200 Off

(Valid until 15 May 2026, 23:59 GMT)

£100 Off

(Valid until 31 May 2026, 23:59 GMT)

For Organisations Outside of Singapore
Get Your Ticket
For Organisations  Based in Singapore
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SERVICE & SOLUTION PROVIDER
Starting from £2895 (+ VAT)

Attendance Only

Partnership benefits not included

Priority Access

Discount automatically applied at checkout to secure preferrential rates

*Standard ticket pricing is £3195+VAT. From 01 June 2026, standard pricing will apply

£300 Off

(Valid until 31 May 2026, 23:59 GMT)

For Organisations  Based in Singapore
Get Your Ticket
For Organisations Outside of Singapore
Get Your Ticket
For Organisations  Based in Singapore
Get Your Ticket

Registration

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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.

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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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