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Join biopharma logistics leaders to explore cold chain innovations and supply chain solutions. Features keynotes, panels, and networking.
Join us at the 9th BioLogistics World Asia 2025 on March 12-13 at Marina Bay Sands, Singapore, where leaders in biopharma logistics come together to address the evolving challenges of transporting biological materials.
This event will delve into the latest strategies and technologies transforming cold chain logistics and strengthening supply chains in Asia's expanding biopharma market. With keynote presentations, panel discussions, and networking opportunities, attendees will explore innovations in cold chain logistics, ensuring the successful delivery of biologics, vaccines, and cell therapies across the region. Don’t miss your chance to shape the future of biopharma logistics in Asia!
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BioLogistics World Asia 2025
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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.
Siang-Chueng Koo is the Director, Innovative Medicine Regulatory Compliance at Johnson & Johnson, where she leads the quality compliance program for J&J manufacturing sites, marketing companies and distribution centers in the 14 Asia Pacific markets. Proficient with global GMP, GCTP and GDP requirements, Siang also has a special interest on cell therapy. Siang has 30 years of experience in the pharmaceutical sector in quality compliance, supply chain, procurement and consulting. As an Asian Compliance Leader with a Lean Sigma Black Belt, Siang is skilled with driving compliance improvement programs and remediation activities. Before joining Johnson & Johnson, she worked at the Singapore Health Authority (Health Sciences Authority HSA), GSK and Abbott. She was a part-time lecturer at National University of Singapore, holds a Master of Health Services Management from Curtin University of Technology, Australia and a Bachelor of Science (Pharmacy)(Hons) from National University of Singapore.
Dr. Horak brings more than 20 years of experience in the global pharmaceutical industry, predominantly focused on oncology drug development, and is a board-certified medical oncologist. Prior to funding Tikva Allocell, Dr. Horak was Head of Global R&D and Chief Scientific at Tessa Therapeutics, a mid-stage cell therapy company in Singapore. For eight years, he was Chief Medical Officer and Chief Scientific Officer at Symphogen, a clinical-stage antibody company, and President of R&D at Enzon Pharmaceuticals, Inc. Dr. Horak has also held a number of senior research leadership positions in various pharmaceutical companies as well as at the National Cancer Institute (NCI), National Institutes of Health in US. During his career, Dr. Horak has advanced multiple oncology treatments into the clinic, and has successfully led a number of FDA new drug applications.
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*END-USER PRICING IS APPLICABLE to:
Company Profiles: Biopharma, BIG Pharmas, Academic & Research Institutes
Applicable Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations
Standard
*END-USER PRICING IS APPLICABLE to:
Company Profiles: Biopharma, BIG Pharmas, Academic & Research Institutes
Applicable Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations
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*SOLUTION PROVIDER PRICING IS APPLICABLE to:
Company Profiles: Service & Solution Providers, International biopharma, Big Pharma, CDMO/CMOs, Academics and Research Institutes*
Applicable Job Profiles: Business Development, Marketing & Sales
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Contact the IMAPAC to learn about our sponsorship process, rates and more.
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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.
Yes, we have a cancellation and refund policy in place. Please refer to our “Cancellation Policy” on our website for details on how to request a refund if you are unable to attend.
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.