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DACH: Where the world comes to understand what cannot be taught - how a culture of perfection becomes a measurable business advantage.

DACH leads the world in biomanufacturing excellence, achieving an extraordinary 99.2% batch success rate across 45+ facilities
The global average? 94–96%
That 5% difference translates to €20–30 million saved per facility every year
To understand the culture behind perfection.
This cannot be studied in a textbook; it is the unwritten code of DACH manufacturing excellence:
BioManufacturing DACH 2027 is where the world comes to understand what cannot be taught – how a culture of perfection becomes a business advantage.


It’s not just the automation. Everyone can buy that.
It’s not just the investment – though €5 billion is reinvested annually, the highest per capita worldwide.
It’s the culture. 50 years of embedding perfection as the baseline, not the goal. A mindset that transforms every process, every team, and every molecule.
You can buy the technology.
You can copy the processes.
But you cannot import the culture of perfection that took half a century to build.
Join the leaders who define the global benchmark for biomanufacturing success; join BioManufacturing DACH 2027 for the 99.2% Standard
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View the Key Themes for
Biologics Manufacturing DACH 2027
Register today to secure your ticket.
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.








Dr. John Bridgeman is an accomplished immunotherapy and cell therapy expert with nearly two decades of experience advancing innovative cancer immunotherapies from early scientific discovery through translational and clinical development. He currently serves as Chief Scientific Officer at ImmunoKey, where he leads the company’s scientific strategy focused on developing next-generation CAR-T therapies designed to address the challenges of treating solid tumours.
Dr. Bridgeman holds a PhD from The University of Manchester, where his research focused on understanding the signalling biology of chimeric antigen receptors (CARs) in T cells. His work contributed to uncovering novel insights into CAR transmembrane domain function and T-cell receptor interactions, laying an important scientific foundation for the advancement of engineered cell therapies. He later continued his scientific training at Cardiff University, contributing to the development of viral-specific T-cell receptor assays and lentiviral engineering technologies for T-cell modulation.
Over the course of his career, Dr. Bridgeman has held leadership roles across several cell therapy and biotechnology organisations, including Instil Bio, Immetacyte Ltd., and Cellular Therapeutics Ltd., where he led research teams focused on novel gene engineering strategies, translational immunotherapy programmes, and CAR-T platform development. His expertise spans T-cell engineering, immuno-oncology, translational science, intellectual property strategy, and advancing innovative therapies toward clinical application.
At ImmunoKey, Dr. Bridgeman is leading the development of the company’s proprietary CARKey™ platform, a multi-specific CAR-T technology designed to overcome tumour antigen heterogeneity and improve the effectiveness of CAR-T therapies in solid cancers. His work focuses on developing safer, more targeted, and more durable cell therapies capable of addressing some of the most significant limitations currently facing solid tumour immunotherapy.
Widely recognised within the advanced therapies and immuno-oncology community, Dr. Bridgeman is a regular speaker at international scientific conferences and industry forums discussing the future of CAR-T therapies, cell engineering technologies, and translational immunotherapy innovation.












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.
Super Early Bird Rate : £1,999.00
Use discount code: SEB
(Valid until 25th September 2026)
Early Bird Rate : £2,199.00
Use discount code: EB
(Valid until 6th November 2026)
Registration Open Rate : £2,399.00
Use discount code: RO
(Valid until 18th December 2026)
Classic Rate : £2,599.00
Use discount code: CR
(Valid until 29th January 2027)
Standard Rate : £2,799.00
Applicable to company profiles
(headquartered outside of the APAC region):
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality.
Early Bird Rate : £2,899.00
Use discount code: EBVD
(Valid until 6th November 2026)
Registration Open Rate : £3,299.00
Use discount code: ROVD
(Valid until 18th December 2026)
Classic Rate : £3,599.00
Use discount code: CRVD
(Valid until 29th January 2027)
Standard Rate : £3,899.00
Applicable to company profiles:
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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 organisations.
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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JUNMIN PENG
IMAPAC