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The 5th ANZ Biologics Festival 2027 unites biopharma leaders to advance Australia & New Zealand's biologics industry through innovation partnerships and manufacturing expansion.
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Excellence in Biologics Manufacturing, Cell and Gene Therapy, and RNA Therapeutics for Australia & New Zealand's Future Biologics Industry.
With a biotechnology sector benchmarked for global excellence due to world-class facilities, researchers, and regulation, the ANZ region has a promising future for biologics innovation and manufacturing. The path ahead will require a focus on further commercial translation of research, and as such, partnerships and collaborations will be critical. Expanding sovereign manufacturing in Australia & New Zealand will also play a massive role in uplifting the sector in the region.
The 5th annual ANZ Biologics Festival 2027 is the region's premier conference that aims to gather the innovators, pioneers, and leaders in the biologics fraternity, including Biologics, Biosimilars, Vaccines, Cell and Gene Therapy (CGT), and RNA Therapeutics, to showcase the latest from ideation to commercialization phase and beyond. It provides the right environment to meet the entire biopharma fraternity under one roof.
Join us to bring investment to Australia & New Zealand's bio sector and explore a wealth of opportunities in biologics innovation, expanding the region's manufacturing footprint, and advancing cell and gene therapy and RNA therapeutics. The 2027 festival will feature dedicated tracks on Biologics Manufacturing, Cell and Gene Therapy, and RNA Therapeutics, offering a comprehensive view of the latest advancements and challenges in these critical areas.
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ANZ Biologics Festival 2027
Explore the latest advances in biologics R&D, from monoclonal and bispecific antibodies to fusion proteins and next-generation therapies transforming biopharmaceutical innovation.
Learn how single-use systems, digital tools, and scalable processes are driving higher efficiency, flexibility, and quality across biologics manufacturing.
Gain practical insights into early-phase clinical trials in ANZ, adaptive trial designs, faster regulatory pathways and alignment with global standards.
Discover strategies in cold chain logistics, smart packaging, and real-time temperature monitoring to strengthen biologics delivery networks.
Explore the latest tools supporting biologics production, from GMP testing and automated quality control systems to advanced analytical technologies and comparability studies.
See how AI, digital twins, and smart automation are reshaping biologics operations through predictive maintenance and process optimisation.
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.


Jase is co-founder and Chief Scientific Officer of Proxima Bio, where he leads scientific strategy, pipeline development and translational research. Trained as a structural biologist and crystallographer, he has expertise in protein and antibody engineering, molecular biology and biochemistry. His work focuses on developing cell-surface degraders as a new class of biologic medicines for autoimmune and inflammatory disease.


Antiksha Joshi is a quality management professional with a deep passion for helping life science organisations implement proactive quality systems that increase regulatory compliance and improve productivity. Having worked for over 25yrs with different types of life science organisations, especially small to mid-sized, she has firsthand experience in the challenges of remaining compliant and efficient in a dynamic ecosystem. It is this experience that she brings to her consulting work - supporting companies build systems, procedures & controls that ensure continued compliance and smoother business operations.
She has helped biotech startups, manufacturing organisations and clinical trial organisations design and implement quality systems customised to their operations & compliance requirements.
Antiksha holds a Master’s in Microbiology as well as a Diploma in Counselling.
Title of the session: From Concept to Capacity: Navigating the Intersection of Innovation, Investment, and Sustainable Growth - The GPN Story


Pete Tobin is Vice President and Head of Translational Medicine at Telix, where he is establishing and leading an Australia-based translational medicine function. Previously based in Boston, Pete served as Senior Vice President, Clinical Strategy and Innovation at Telix, where he oversaw clinical development strategy across the company’s portfolio. He brings over two decades of experience collaborating with academic, clinical, and industry partners to translate novel oncology science into new treatment options for patients.




David Haylock is a stem cell biologist who jointly pioneered mobilised blood stem cell transplantation and associated mobilisation strategies and apheresis procedures that are the basis for treatments of blood cell cancers and other diseases.
Haylock developed the concept of ex vivo expansion of haemopoietic stem cells to generate cells for therapy and, as Head of Experimental Cell Therapy at the Peter MacCallum Cancer Centre in Melbourne, led Australia’s first clinical trial with GMP, ex vivo expanded CD34+ cells in the setting of repetitive high dose chemotherapy for metastatic breast cancer.
Haylock was appointed as the CSO of VivaZome Therapeutics in January 2018. In this role Haylock has developed a universal extracellular vesicle (EV) manufacturing process and a suite of analytics and potency assays for EV therapeutics.
Haylock has initiated and secured multiple collaborative partnerships with academic research groups, Australian SMEs and national and multinational biotech and pharma companies to evaluate a diverse range of technologies, materials, and assays for EV manufacture.




Paul is an established pharmaceutical/biotech CEO with over 25 years in pharmaceutical product development, operations, and business development. He holds postgraduate qualifications in Biomedical and Business studies. Paul is the current CEO of RNA Australia and has led senior roles at Pfizer and IDT Australia. Paul is recognised for driving innovation to successful commercialisation, building strong stakeholder relationships, and delivering long-term growth.


Dr Rebecca Lim is Chief Scientific Officer at INOVIQ Ltd (ASX:IIQ) with more than two decades of experience translating cell, gene and extracellular vesicle technologies from discovery through clinical development. Her career spans academic research, GMP cell therapies, early phase clinical translation, industry strategy and cross-functional program leadership. Rebecca previously held senior industry roles at CTMC (Houston, Texas) and at Monash University and the Hudson Institute of Medical Research, where she pioneered clinical translation of placental cell and exosome-based therapeutics. At INOVIQ, she leads scientific and development strategy across the company’s EV diagnostics and therapeutics programs.


Associate Professor Shayanti Mukherjee is Head of the Translational Tissue Engineering Laboratory at Hudson Institute of Medical Research and an Emerging Leader in Women’s Health. Her research integrates biomaterials, immune engineering, and regenerative medicine to develop next-generation therapies for pelvic floor disorders following childbirth injury. She leads translational programs spanning degradable surgical meshes, biological grafts and cell-derived regenerative therapies, validated across small and large animal models with a clear pathway to clinical impact. She is a recipient of the SIEF John Stocker Fellowship and Johnson & Johnson WiSTEM2D Scholar, and is a passionate advocate for equity and inclusion in STEM.


Silvio Tiziani is Chief Executive Officer of the Centre for Commercialisation of Regenerative Medicine (CCRM) Australia, where he leads initiatives focused on accelerating the translation, commercialisation and scaling of advanced therapies. With extensive international experience across biotechnology, healthcare, commercialisation and investment, he works closely with industry, researchers, governments and investors to strengthen Australia's regenerative medicine and advanced therapies ecosystem. Through CCRM Australia, Silvio is focused on building the partnerships, infrastructure and investment pathways required to support innovation, manufacturing growth and improved patient access to transformative therapies.
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.
Early Bird Rate : SGD 1,495
Use discount code: EARLYBIRD
(Valid until 5th September 2026)
Registration Open Rate : SGD 1,695
Use discount code: REGISTRATIONOPEN
(Valid until 7th November 2026)
Standard Rate : SGD 1,895
Use discount code: STANDARD
(Valid until 9th January 2027)
Final Call Rate : SGD 2,095
Applicable to company profiles (headquartered within the ANZ region):
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations.
Early Bird Rate : SGD 1,995
Use discount code: EARLYBIRD
(Valid until 5th September 2026)
Registration Open Rate : SGD 2,195
Use discount code: REGISTRATIONOPEN
(Valid until 7th November 2026)
Standard Rate : SGD 2,395
Use discount code: STANDARD
(Valid until 9th January 2027)
Final Call Rate : SGD 2,595
Applicable to company profiles (headquartered outside of the ANZ region):
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations
Early Bird Rate : SGD 2,995
Use discount code: EARLYBIRD
(Valid until 5th September 2026)
Registration Open Rate : SGD 3,195
Use discount code: REGISTRATIONOPEN
(Valid until 7th November 2026)
Standard Rate : SGD 3,395
Use discount code: STANDARD
(Valid until 9th January 2027)
Final Call Rate : SGD 3,595
Applicable to company profiles:
Job Profiles: Business Development, Marketing, and Sales
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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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