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BioSupply Chain Asia 2026
10th Edition
Asia’s #1 Conference for Biologics Supply Chain & Cold Chain Excellence
Join biopharma logistics leaders to explore cold chain innovations and supply chain solutions. Features keynotes, panels, and networking.
Sands Expo & Convention Centre Singapore
11
-
12
March 2026
00
Days
00
Hours
00
Mins
00
Secs
300
+
Attendees
Maximum Attendees
100
+
Companies
20
+
Speakers
48
+
Networking Hours
8
+
Case Studies
Interactive Sessions
About the Event
Be Part of Asia’s Premier Biopharma Logistics Gathering – BioSuppy Chain Asia 2026
Join us for the 10th Annual BioSupply Chain Asia 2026, taking place on March 11–12, 2026, at Marina Bay Sands, Singapore – where the region’s top biopharma logistics leaders converge to drive innovation and resilience in cold chain and supply chain operations across the industry.
As Asia’s biopharma sector continues its rapid expansion, this milestone edition will spotlight next-generation strategies, technologies, and best practices for transporting sensitive biological products — from biologics and vaccines to cell and gene therapies. Featuring insightful keynotes, dynamic panel discussions, and high-impact networking, this is your opportunity to stay ahead of regulatory shifts, digital transformation, and sustainability imperatives in the supply chain.
Celebrate a decade of progress and be part of the conversation shaping the future of biopharma logistics in Asia.
Agenda at a Glance
View the Key Themes for
BioSupply Chain Asia 2026
Day 1 I Resilience, Visibility & Sustainability in Biopharma Logistics
- Leadership Panel: Building Resilient & Future-Ready Biopharma Supply Chains in Asia
- Next-Gen Cold Chain Logistics: Real-Time Visibility with Smart Devices
- Smart Packaging & Traceability for Temperature-Sensitive Biologics
- Driving Sustainability in Cold and Ambient Chain Logistics
- Asia-Pacific Biopharma Excellence Awards 2026 Gala Dinner
Day 2 I Digital Transformation, Clinical Efficiency & Regulatory Readiness
- Smart Supply Chain 4.0: Predictive Logistics, AI, Blockchain & Automation Use Cases
- Transforming Clinical Trial Logistics in APAC [Combined Session for CTFA & BSCA]
- Meeting Regulatory Expectations & GxP Compliance in Asia
- Plenary Roundtable Discussions & Future Outlook [Combined Session]
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.
Dinesh Khokal
Beigene
Global Director, GxP Surveillance & Quality External Affairs, Global Technical Operations
Advisory Board Commitee
Chairman
Dinesh Khokal
Global Director, GxP Surveillance & Quality External Affairs, Global Technical Operations
Beigene
Singapore
Jun Liang Yaw
Hilleman Laboratories
Senior Manager, Supply Chain
Advisory Board Commitee
Chairman
Jun Liang Yaw
Senior Manager, Supply Chain
Hilleman Laboratories
Singapore
Shawn Lim
Santen Pharmaceutical
Senior Manager - Asia Artwork Mgmt + Strategic Projects + Global Artwork Leadership
Advisory Board Commitee
Chairman
Shawn Lim
Senior Manager - Asia Artwork Mgmt + Strategic Projects + Global Artwork Leadership
Santen Pharmaceutical
Singapore
Raneeth Reghu
Biocon Biologics
Senior Director, Procurement & Supply Chain
Advisory Board Commitee
Chairman
Raneeth Reghu
Senior Director, Procurement & Supply Chain
Biocon Biologics
Malaysia
Rosaline Lee
MSD
Associate Director, AP D&L
Advisory Board Commitee
Chairman
Rosaline Lee
Associate Director, AP D&L
MSD
Singapore
Siang-Chueng Koo
Johnson & Johnson
Director, J&J Regulatory Compliance (Innovative Medicine), Asia Pacific
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.
Advisory Board Commitee
Chairman
Siang-Chueng Koo
Director, J&J Regulatory Compliance (Innovative Medicine), Asia Pacific
Johnson & Johnson
Singapore
Josiane Touma
Pfizer
Supply Chain Director
Advisory Board Commitee
Chairman
Josiane Touma
Supply Chain Director
Pfizer
UAE
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.
Registration
Choose a plan that fits your role, company, and industry.
BioPharma & Academic Based in Asia
Starts from SGD 1,495
Early Bird Rate : SGD 1,495
(Valid until 2nd October 2025)
Registration Open Rate : SGD 1,695
(Valid until 4th December 2025)
Standard Rate : SGD 1,895
(Valid until 5th Feb 2026)
Final Call Rate : SGD 2,095
(Valid until 11th March 2026)
Applicable to company profiles (headquartered within the APAC region):
- BioPharma
- Academic Institutions
- Research Organisations
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations
BioPharma & Academic Based Outside of Asia
Starts from SGD 1,995
Early Bird Rate : SGD 1,995
(Valid until 2nd October 2025)
Registration Open Rate : SGD 2,195
(Valid until 4th December 2025)
Standard Rate : SGD 2,395
(Valid until 5th Feb 2026)
Final Call Rate : SGD 2,595
(Valid until 11th March 2026)
Applicable to company profiles (headquartered outside of the APAC region):
- BioPharma
- Academic Institutions
- Research Organisations
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations
Big Pharma & Solution Providers
Starts from SGD 4,295
Early Bird Rate : SGD 4,295
(Valid until 2nd October 2025)
Registration Open Rate : SGD 4,495
(Valid until 4th December 2025)
Standard Rate : SGD 4,695
(Valid until 5th Feb 2026)
Final Call Rate : SGD 4,895
(Valid until 11th March 2026)
Applicable to company profiles:
- Big Pharma
- Technology, Service, and Solution Providers
- CDMO/ CMO
Job Profiles: Business Development, Marketing, and Sales
Registration
Register Your Interest
Be the first in line! Register your interest now to get exclusive access to Super Early-Bird tickets - the lowest prices available - before they go live.
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Want to Sponsor This Event?
Contact the IMAPAC to learn about our sponsorship process, rates and more.
Pre Conference Workshops & Other Sessions
Visit the event page to view more content.
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Co-Located Events
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Awards Cerermony
Visit the awards page to view more content.
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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.
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.
Is there a cancellation or refund policy if I can't attend after registering?
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.
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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Don't miss out on unique networking, speaking and sponsorship opportunities.