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Where regulatory pioneers, operations leaders, digital quality architects, and manufacturing strategists come together to accelerate biologics manufacturing innovation; from flexible regulatory sandboxes to digital quality frameworks and future workforce strategies.

Biologics Manufacturing UK is the industry’s focal forum for practical, outcome-driven dialogue on how biologics and advanced therapies will be manufactured reliably, compliantly, and at scale in the UK and beyond.
The UK’s regulatory landscape, including world-first sandbox frameworks for decentralised and modular manufacturing, is redefining what’s possible in point-of-care and flexible production. At the same time, Digital Quality Anchors such as AI-enabled QMS, Digital Twins, and Real-Time Release Testing (RTRT) are becoming essential foundations for data integrity and cross-border compliance. Meanwhile, unprecedented capacity expansion and strategic workforce evolution are turning the facilities of the future into operational realities.
This is not a theoretical showcase. This is where senior leaders shaping biologics manufacturing translate innovation into execution.


If your role touches on getting biologics production from concept through compliant, scalable manufacture, this is where those problems get solved.
Navigating the UK’s world-first regulatory frameworks for decentralised, modular and point-of-care biologics manufacturing, including control site models that separate oversight from production to enable flexible, compliant systems
Exploring how AI-driven Quality Management Systems, Digital Twins, and Real-Time Release Testing are creating digital compliance firewalls that protect data integrity and support scalable, networked supply chains
Addressing the real challenges of expanding biologics manufacturing capacity while closing the skills gap: from strategic staffing models to next-gen training initiatives that prepare teams for advanced therapies and modular production systems
Practical frameworks for embedding resilient quality systems, harmonised data ecosystems, and scalable manufacturing processes that align with UK regulatory expectations and global supply chain requirements
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Biologics Manufacturing UK 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.
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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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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.
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.
Don't miss out on unique networking, speaking and sponsorship opportunities.