10th Annual Clinical Trial Supply Korea 2025

From global supply chain trends to Korea-specific solutions discover how to streamline processes, reduce delays, and transform the future of clinical trial supply

2 - 3

December

2025
  • JW Marriott Dongdaemun Square Seoul, South Korea
  • Ticketed
  • Why attend?
  • Agenda
  • Advisory Board
  • Speakers
  • Plan Your Visit
  • Event Gallery
  • 2025 Sponsors
  • Media Centre
  • Presentations
  • Why partner?
  • Contact Us
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2025 Sponsors Include:

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Company Information

Novotech is a globally recognized full-service clinical research organization (CRO) and scientific advisory partner for biotech and small- to mid-sized pharmaceutical companies seeking to advance drug development. With deep therapeutic and regulatory expertise and an expansive global footprint across the Asia-Pacific region, North America, and Europe, Novotech offers clients an accelerated path to bring life-changing therapies to market.

Company Website

To learn more, please visit our website - www.novotech-cro.com

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N-SIDE is a deeptech company that empowers organizations in the life sciences to make better decisions and optimize the use of critical resources. We’re doing so by combining deep industry expertise with applied mathematics and artificial intelligence into easy to use and cutting-edge software that transforms uncertainty and complexity into deterministic outcomes. We are an active player in clinical trial supply chain management for over 20 years and have the majority of the top 20 pharmaceutical companies as clients.

With our software solution, the N-SIDE Suite, and expert services, we streamline the clinical supply of pharmaceutical and biotech companies by accelerating clinical plans, mitigating risks and curbing drug waste. We empower clinical leaders to make better, faster and safer decisions for patients waiting for life-changing medications.

Company Website

To learn more, please visit our website - https://lifesciences.n-side.com/

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Company Information

Akesa is an end-to-end provider of clinical trial supplies and services. Headquartered in Melbourne, Australia, Akesa boasts global reach with deep expertise in the Asia-Pacific region. We work alongside sponsors, CROs, research institutions, clinical trial sites and CDMOs to project manage the sourcing of finished products, including comparators, combination therapies, and standard-of-care medications, from validated suppliers and directly from manufacturers.

Company Website

To learn more, please visit our website - http://akesapharma.com/

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360biolabs is Australia’s most comprehensive bioanalytical laboratory providing support for development of new therapeutics, vaccines and diagnostics. We support pharmacokinetic (PK) analysis, pharmacodynamic (PD) endpoints in a quality assured environment (GLP, GCP, ISO / IEC 17025). We provide the advantage of a Phase 1 solution in Australia and transfer or continuation of your clinical study with our team in the USA or Europe.

The benefits of conducting early phase clinical trials in Australia: 

  • Speed: No IND required, healthy volunteer study approval in ~4-6 weeks
  • Quality: Data recognized by global regulatory bodies (e.g. FDA, EMA)
  • Cost-Effectiveness: Up to 43.5% R&D tax incentive

Company Website

To learn more, please visit our website - http://www.360biolabs.com/

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Company Information

Almac Group is a global leader in providing a range of expert services and support across the drug development lifecycle.

We are trusted experts in R&D, diagnostic services, API manufacture, formulation development, clinical trial supply services and technologies through to commercial-scale manufacture and distribution.

We are recognised as an industry leader in client service, providing understanding, experience and knowledge to our clients as we work together to advance human health.

Almac is trusted by the leading global biopharma companies to provide crucial services across their drug development projects. In the last 5 years alone, we have contributed to over 50% of all FDA approved New Molecular Entities (NMEs) and are currently supporting 30% of EU approved /pre-registered Gene therapy products.

A privately owned organisation, Almac has grown organically over the past five decades, employing over 7,700 highly skilled employees across 18 facilities in Europe, North America, and Asia. Learn more about us at https://www.almacgroup.com/

Company Website

To learn more, please visit our website - https://www.almacgroup.com

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Company Information

BMclinical, your global clinical trial supply partner. We offer worldwide commercial medicine supply, from analytical samples to bulk comparators, through to the supply of co-meds and pre-meds.  We can pack and label your IMP/commercial medicines from our GMP facility, where we also offer storage and distribution services. BMclinical is uniquely positioned to offer solutions for overage and unused clinical trial stock.

Company Website

To learn more, please visit our website - https://www.bmclinical.com

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Company Information

Complex innovative clinical trial designs require a synergetic approach to assess novel drug compounds for safety and effectiveness which often span safety, regulated and esoteric outcomes in all phases of the drug development life cycle. The companies of Eurofins Bioanalytical Services, the Eurofins Central Laboratory global network, Eurofins Viracor BioPharma Services, and Eurofins Clinical Trial Supplies are strongly connected to provide a solutions-based approach to our client needs.  Eurofins Clinical Trial Solutions provides seamless, end-to-end solutions to help clients progress through the drug development cycle through a single, experienced provider. Our solutions deliver the most comprehensive range of state-of-the-art analytical technologies with an extensive geographic reach to support our clients’ testing and clinical supplies needs and stringent quality and safety requirements around the world.

Company Website

To learn more, please visit our website - https://www.eurofins.com/biopharma-services/clinical-trial-solutions/

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Company Information

George Clinical is a leading CRO in Asia Pacific, with unparalleled Investigator networks. Since 1999, we have been providing full trial management services to biopharmaceutical customers. George Clinical combines

Company Website

To learn more, please visit our website - www.georgeclinical.com

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Scout empowers the life sciences industry with people-first solutions: Scout Meetings, Scout Clinical, and Scout Academy. We specialize in face-to-face, virtual, and hybrid clinical meeting planning, patient payment, travel, and logistics support, and virtual collaboration and education. Since 1995, we have been a trusted partner excelling in customer service, regulatory compliance, and project delivery for leading pharmaceutical and biotechnology companies. Our deep understanding of international regulations and adaptable network of resources is built on operational experience in 109 countries. With white-glove attention to detail and a customizable, comprehensive range of services, Scout makes the complex easier. Learn more at scoutclinical.com.

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Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,000 people across 44 countries.

Company Website

To learn more, please visit our website - http://www.medpace.com/

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Company Information

QPS is a global contract research organization (CRO) providing discovery, preclinical and clinical drug development services since 1995. Our mission is to accelerate pharmaceutical breakthroughs across the globe by delivering custom-built research services. An award-winning leader focused on bioanalytics and clinical trials, QPS is known for proven quality standards, technical expertise, a flexible approach to research, client satisfaction and turnkey laboratories and facilities. We are passionate about our work, creating value for patients and customers while generating opportunities for employees to thrive.

Company Website

To learn more, please visit our website - www.qps.com

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Company Information

Euromed Pharma deliver strategic services tailored to support companies in their quest to better healthcare. We support each industry player from drug development through the post-marketing phases. We offer solutions in CTS services, Clinical GMP Packaging, Labeling and Distribution, IMP management, Early Access and Named Patient Programs, Pharma Order to cash solutions, and Supply Chain & Logistics. We are present around the world with offices in Italy, Spain, Ireland, Germany, Singapore and the USA. Being one of the Petrone Group companies, Euromed Pharma is positioned at the forefront of innovation in pharmaceutical distribution.

Company Website

To learn more, please visit our website - www.euromed-pharma.com

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    Why attend?

    The leading  Clinical trials supply conference in Korea is returning in 2025. With a focus on providing delegates with practical take-aways and solutions to their most current operational and outsourcing challenges in clinical trials, this is an event not to be missed.

    Why join?

    Unlike other conferences, our event focuses especially on the regional pharmaceutical business in Asia, highlighting the industry’s current difficulties as well as its exciting innovations and growth prospects.

    Not only will the audience be discussing clinical partnership and supply challenges, but we also have the Outsourcing Clinical Trials Korea conference co-located with the event to give you the opportunity to define an end-to-end clinical strategy.

    Meet and network with over 250 senior industry decision makers during our dedicated networking breaks, round tables and interactive sessions.

    Agenda

    • 2 Dec 2025
    • 3 Dec 2025
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    8 AM

    Registration and refreshments

    8:40 AM

    Chairperson’s opening remarks

    8:45 AM

    How to Choose the Right Clinical CRO: A Strategic Guide for Biotech Venture

    ·        Determining the optimal stage for CRO engagement to maximize efficiency

    ·        Engaging CROs in protocol development to inform strategic decisions, including country selection and trial design considerations

    ·        Leveraging CRO expertise by fostering a collaborative, partnership-driven relationship

    Speakers

    Sol Han
    Chief Medical Officer, Head of Clinical Development Center, Cyrus Therapeutics

    9:15 AM

    Reserved for Novotech

    9:45 AM

    KEY NOTE: Why Listening to Patients Matters: Redefining Clinical Development Strategies

    ·        Understanding how prioritizing patient care enhances trial success

    ·        FDA guidance driving patient-centric clinical development

    ·        Real-world impact of patient input on protocol design and trial conduct

    Speakers

    Kazuhiko Takahata
    Senior Director, Head of Clinical Development Group 3, Clinical Development Centre, Kyowa Kirin(Japan)

    10:15 AM

    Reserved for the Event Partner

    10:45 AM

    Morning refreshments and networking

    11:30 AM

    Advancing Adaptive Strategies for Clinical Trial Supply Manufacturing

    ·        Strategies for just-in-time manufacturing to reduce inventory and waste

    ·        CMO Selection: Aligning Partner Capabilities with Evolving Clinical Supply Demands

    ·        Modernizing the Supply Chain: Evaluating and Adopting Next-Generation Manufacturing Solutions

    Speakers

    Sangho Ma
    VP Development , A&J science

    12 PM

    Reserved for Akesa Pharma

    12:30 PM

    Optimizing Central Lab Supply Chains: Overcoming Logistical Barriers in Clinical Sample Management

    ·        Addressing challenges in collection, labeling, packaging, and international shipping

    ·        Ensuring cold chain integrity to maintain sample viability and data accuracy

    ·        Navigating cross-border requirements, permits, and documentation delays

    Speakers

    Jaeyoung Hyun
    Unit Manager, GCCL

    1 PM

    Lunch and networking

    2:15 PM

    GMP and Global Trials: Managing Multi-Regional Requirements for Manufacturing and Labeling

    ·       Ensuring quality and documentation consistency through effective CMO/CDMO coordination

    ·       Harmonizing GMP standards across regions with differing regulatory expectations

    Speakers

    Jung Won Jung
    Production Team Manager, inno.N

    2:45 PM

    Reserved for the Accmed Technology

    3:15 PM

    Streamlining Success: An Integrated Approach to Clinical Quality Assurance in Supply Chains

    ·        Regularly auditing suppliers and manufacturing partners to ensure compliance with regulatory standards

    ·        Conducting regular training and workshops to align all parties on quality assurance standards and practices

    ·        Developing and maintaining detailed risk management plans

    Speakers

    Alicia Kim
    Clinical Trials Team Leader, LN Robotics

    3:45 PM

    Afternoon refreshments and networking

    4:15 PM

    Managing Investigational Product (IP) in Clinical Trials: Best Practices for Compliance, Safety, and Efficiency

    ·        Points to consider in relation to Investigational Product(including comparator) when conducting clinical trials

    ·        Key Strategic Exploration for Efficient Supply and the use of IRT

    ·        Discussing effective risk management strategies to anticipate and mitigate potential challenges, ensure uninterrupted supply, and minimize delays

    Speakers

    HyeJung Yang
    Clinical Development Center, Clinical Team Lead, Daewoong Pharmaceutical

    4:45 PM

    PANEL DISCUSSION: Stronger Together: Mastering Vendor Relationships for Game Changing Clinical Supply Results

    ·        Cultivating trust and shared value through End-to-End clinical supply chain collaboration

    ·        Creating effective communication channels to enhance transparency and strengthen trust

    ·        Aligning incentives between sponsors and vendors to prevent supply shipment delays

    Speakers

    Priya Ravisekara
    Senior Pharma Analyst, GlobalData Plc
    HyeJung Yang
    Clinical Development Center, Clinical Team Lead, Daewoong Pharmaceutical
    Alicia Kim
    Clinical Trials Team Leader, LN Robotics

    5:15 PM

    Chairperson’s closing remarks

    8:15 AM

    Registration and refreshments

    8:50 AM

    Chairperson’s opening remarks

    9 AM

    Insights and Lessons Learned from Managing Clinical Supply Chains for Cell and Gene Therapies

    • Cell and gene Therapy in clinical supply key differences and strategic considerations
    • New technology and advances
    • Case examples highlighting compliance challenges

    Speakers

    Priya Ravisekara
    Senior Pharma Analyst, GlobalData Plc

    9:30 AM

    Reserved for the Event Partner

    10 AM

    Streamlining the End-to-End pharmaceutical supply Chain: Enhancing efficiency and quality

    • Understanding the complexities and challenges of the end-to-end pharmaceutical supply chain, from manufacturing to patient delivery
    • Addressing regulatory requirements and compliance
    • How did we implement effective strategies to enhance the end-to-end pharmaceutical supply chain

    Speakers

    Hyesung Shin
    Director, Clinical Development Strategy, R&D Division, Aptabio

    10:30 AM

    IATA Temperature Control Regulations (TCR) on Clinical trials supply chain

    • Influence of TCR (Time, Temperature, and Condition) on Pharmaceutical Transportation
    • Effective Application of Time and Temperature Sensitive Labels
    • Ensuring Compliance with TCR Regulations in Clinical Trials

     

    Reserved for IATA

    11 AM

    Morning refreshments and networking

    11:45 AM

    Why do clinical supply also require shipping validation

    • Overview of recent changes in regional regulations.
    • Supplier management
    • Shipping validation case study

    Speakers

    Seunghyun Hong
    Logistics Manager, GCBiopharma

    12:15 PM

    PANEL DISCUSSION: Turning Transit Troubles into Triumphs: Proven Strategies for Clinical Supply Success

    • Common causes of transit issues: shipment delays, temperature excursions, customs holds, and packaging failures
    • Addressing gaps in global regulatory guidance
    • Practical solutions for streamlining supply chain processes

     

    Speakers

    Priya Ravisekara
    Senior Pharma Analyst, GlobalData Plc
    Hyesung Shin
    Director, Clinical Development Strategy, R&D Division, Aptabio

    1 PM

    Lunch and networking

    Prize Draw taking place in exhibition hall at 14:15

    Join us for a chance to win one of our prizes, including Apple products

    2:30 PM

    KEY NOTE: Driving CRO Performance in Clinical Trials

    • Determining the optimal stage for CRO engagement to maximize efficiency
    • Engaging CROs in protocol development to inform strategic decisions, including country selection and trial design considerations
    • Leveraging CRO expertise by fostering a collaborative, partnership-driven relationship

    Speakers

    Eunah Paek
    Executive Director, Boryung corporation

    3 PM

    Speaker Hosted Roundtables

    Interactive roundtable sessions offer a unique opportunity to come together with your peers to share best practice and develop solutions to critical challenges facing the industry as a whole. Hosted by industry experts and each focused on a single issue, roundtables are an exciting, interactive way to build your personal network and learn from the experience and expertise of others.

    Roundtable session lasts for 30 minutes and rotate

    ROUNDTABLE 1: Comparator Sourcing in Small Biotech: Overcoming Limits with Strategic Outsourcing
    ROUNDTABLE 2: Driving Efficiency and Results Through Strong Sponsor, CRO Partnerships

    YongGwan Kim, Associate Director, Janssen
    ROUNDTABLE 3: Key Areas to Focus on for Proactive Inspection Preparedness in Today’s Regulatory Landscape
    ROUNDTABLE 4: Integrating Packaging and Labeling with Clinical Supply Chain Operations

    3:30 PM

    Chairperson’s closing remarks

    END OF CONFERENCE

    Speakers

    Select a speaker to learn more

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    Priya Ravisekara
    Senior Pharma Analyst, GlobalData Plc

    Priya Ravisekara, MSc,is a senior analyst at GlobalData in London, UK, where her primary responsibilities include producing analytical reports, improving and maintaining database functionality through quality assurance testing, updating and monitoring Global Data’s Clinical Trials Intelligence Database, and answering queries directly from clients. Priya holds a Masters in Clinical Drug Development from Barts and The London School of Medicine and Dentistry, and a Bachelor of Science in Biochemistry from Brunel University, London.​

    Session Details:

    PANEL DISCUSSION: Stronger Together: Mastering Vendor Relationships for Game Changing Clinical Supply Results

    2025-12-02, 4:45 PM

    Session Details:

    Insights and Lessons Learned from Managing Clinical Supply Chains for Cell and Gene Therapies

    2025-12-03, 9:00 AM

    Session Details:

    PANEL DISCUSSION: Turning Transit Troubles into Triumphs: Proven Strategies for Clinical Supply Success

    2025-12-03, 12:15 PM

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    Sangwoo Lee
    CEO, Jeju Biotek

    With 16 years of experience in the pharmaceutical industry, including over 5 years in non-clinical pharmacology and nearly a decade in clinical development, Sangwoo Lee has managed more than 10 clinical studies across both international sites (United States, Australia, Indonesia, and Singapore) and domestic settings in South Korea.

    Specialties

    Full Scoped Clinical Development

    Clinical trial operation management and supervision based on Regulations and ICH guidelines

    Development of IND CTD module relevant for Clinical Trial and Nonclinical Study

    Planning and Management of Clinical Study Timeline and Budget

    Vendor Selection and Management (CRO, Analytical Lab, Couriers)

    Study Site Management and communication

    IMP Management (Blinded)

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    Young Su (Bobby) Noh
    Director, Head of Clinical Research and Development (ONCO),Hanmi Pharm

    Young Su (Bobby) Noh, Ph.D., is the Director, Clinical Research and Development (Oncology), Hanmi Pharma and a representative of IFPMA, ICH E22 informal Expert Working Group. Dr. Noh is also working as a committee member of KIC2025, an external Instructor in KoNECT and a reviewer of external evaluation committee of KDDF. Dr. Noh has been responsible for leading clinical program with NMEs or NBEs in multi-therapeutic area: including metabolic diseases and rare diseases as well as oncology and hematology for 17 years. Dr. Noh has a lot of experience for collaborating with global big pharma as well as biotech companies.

    Previously, Dr. Noh served as an adjunct professor, department of regulatory science for Kyung Hee university and an expert, several guidelines Working Group of MFDS. Dr. Noh received his Ph.D. in pharmacy Kyung Hee University.

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    Kazuhiko Takahata
    Senior Director, Head of Clinical Development Group 3, Clinical Development Centre, Kyowa Kirin(Japan)

    Experienced clinical development leader with a proven record in strategic decision-making and cross-functional team leadership within global pharmaceutical organizations.

    Expertise spans immunology, oncology, and allergy therapeutic areas, with deep experience in cross-border regulatory engagement and clinical trial execution.

    Combines scientific rigor with a business-focused mindset, currently pursuing a PhD in health economics to further strengthen academic and strategic capabilities.

    Session Details:

    KEY NOTE: Why Listening to Patients Matters: Redefining Clinical Development Strategies

    2025-12-02, 9:45 AM

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    Jongyeop (Peter) Kim
    Lead Manager, Big Data Team, Daewon pharmaceutical

    Education: Department of Business, Tourism and Accounting, Major in Business Administration, Kangwon National University

    Career: Daewon Pharmaceutical Co Ltd (Medical Representative - Distribution Manager - Sales Planner - Big Data Specialist)

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    YOHAN BAE
    Executive Director, Clinical Development Division, Kangstem Biotech

    Yohan Bae is Executive Director, Clinical Development Division at Kangstem Biotech Co. Ltd since he joined in Mar 2020. He has almost 30 years of drug development experience ranging local and global regulatory affairs, clinical development, and patient access for pharmaceutical and medical device. Before he joined in Kangstem Biotech, Mr. Bae has worked for large international pharma and medical device companies such as Alcon, Bristol-Myer Squibb, and Boehringer-Ingelheim. He holds a master’s degree in Pharmacology from Pharmacy College, Kyunghee University.

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    Eunah Paek
    Executive Director, Boryung corporation

    Ms. Eun-Ah Paek, Executive Director at Boryung Co., Ltd., majored in Pharmacy at Sookmyung Women’s University, where she also earned her Master’s degree in Pharmacology. She subsequently completed her doctoral coursework in Pharmacoepidemiology at Sungkyunkwan University.

    She previously served as a project leader for central nervous system (CNS) drug development at SK Biopharm and is currently in charge of clinical trials, post-marketing clinical research, pharmacovigilance, and medical writing as the head of the Clinical Division at Boryung.

    With over 30 years of experience, she has been involved in comprehensive drug development, spanning from non-clinical research to clinical trials and post-marketing activities for pharmaceuticals.

    Session Details:

    KEY NOTE: Driving CRO Performance in Clinical Trials

    2025-12-03, 2:30 PM

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    Choong Hee LEE
    Director, Clinical Development, Vasthera
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    Amy Jung Hyun LEE
    Medical imaging expert

    Amy is a seasoned imaging clinical trial expert with a PhD in Biomedical Sciences and extensive experience in the design, execution, and evaluation of imaging across multiple therapeutic areas, including oncology, ophthalmology, neurology, dermatology, musculoskeletal, and gastroenterology. With nearly a decade of leadership in managing imaging projects, she has worked with global pharmaceutical companies, leading CROs, and major hospitals worldwide. Her career journey spans roles from imaging project manager to CEO of a Singapore-based imaging CRO, and she now brings her expertise to a global imaging CRO.

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    Jaeyoung Hyun
    Unit Manager, GCCL

    Jaeyoung Hyun serves as Head of the Business Development Unit at GCCL(Global Clinical Central Lab), a leading central lab in Asia Pacific specializing in clinical trial sample analysis for global pharmaceutical and biotech sponsors. In this role, he oversees domestic and global client engagement, strategic sales, and partnership development, driving GCCL’s growth and international presence.

    With a long-standing career in domestic sales and business development within the pharmaceutical and healthcare industries, Mr. Hyun has cultivated deep expertise in fostering client relationships, shaping commercial strategies, and supporting multinational clinical programs. His professional background includes extensive collaboration with pharma and biotech companies, with a focus on overcoming logistical barriers in clinical sample management—an area he will address in his OCT Korea 2025 session, “Optimizing Central Lab Supply Chains: Overcoming Logistical Barriers in Clinical Sample Management.”

    Session Details:

    Optimizing Central Lab Supply Chains: Overcoming Logistical Barriers in Clinical Sample Management

    2025-12-02, 12:30 PM

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    Seunghyun Hong
    Logistics Manager, GCBiopharma

    Session Details:

    Why do clinical supply also require shipping validation

    2025-12-03, 11:45 AM

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    Sangho Ma
    VP Development , A&J science

    Dr. Sang Ho Ma, Ph.D. in Pharmacy, is Vice President of Development at A&J Science and a member of the Expert Committee of the Ministry of Food and Drug Safety (MFDS). With over 20 years of

    experience in drug discovery and development, including CMC, regulatory affairs, and clinical research, he provides expertise across immuno-oncology, rare diseases, infectious diseases, and vaccines.

    Session Details:

    Advancing Adaptive Strategies for Clinical Trial Supply Manufacturing

    2025-12-02, 11:30 AM

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    Sol Han
    Chief Medical Officer, Head of Clinical Development Center, Cyrus Therapeutics
    Sol Han currently serves as the Chief Medical Officer (CMO) and Head of Clinical Development at Cyrus Therapeutics, a company specializing in oncology drug development. In this pivotal role, Sol is spearheading critical phases of drug development, including Investigational New Drug (IND) application submissions, early-stage clinical development, and the successful translational research that bridges non-clinical findings to human clinical trials.
    With a professional background in pharmacy at Ewha Woman’s University, Sol brings two decades of deep industry experience, including 15 years garnered at Global Big Pharma companies such as Roche, GSK, and Sanofi. During this tenure, Sol established a distinguished clinical professional career as a Global Leader, successfully pioneering clinical operations and development not only locally but also globally.
    Leveraging this profound expertise gained within the patient-centric and trend-setting global pharmaceutical landscape, Sol is now at Cyrus Therapeutics, successfully integrating advanced clinical development know-how into the domestic biotech sector and proactively elevating the company's clinical capabilities to a global standard.

    Session Details:

    How to Choose the Right Clinical CRO: A Strategic Guide for Biotech Venture

    2025-12-02, 8:45 AM

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    YongGwan Kim
    Associate Director, Janssen
    • Associate Director-Trial Delivery Leader, Medical Affairs Delivery Unit, J&J Innovative Medicine
    • Masters Degree of Supply Chain Management, MBA, Inha University
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    Alicia Kim
    Clinical Trials Team Leader, LN Robotics

    - 23Y Clinical Trial & New Drug Development Expert Professional

    - Global & Local Trials Experiences including the 1st Phase 2 COVID-19 New Oral-drug Trial PM in Korea & USA

    - Global CROs and Local Pharmacies Experiences

    - All-round Experts in Clinical Trials (Medicines & Devices)

    Session Details:

    Streamlining Success: An Integrated Approach to Clinical Quality Assurance in Supply Chains

    2025-12-02, 3:15 PM

    Session Details:

    PANEL DISCUSSION: Stronger Together: Mastering Vendor Relationships for Game Changing Clinical Supply Results

    2025-12-02, 4:45 PM

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    HyeJung Yang
    Clinical Development Center, Clinical Team Lead, Daewoong Pharmaceutical

    Hyejung Yang is the Team Leader of the Clinical New Drug Team at Daewoong Pharmaceutical. She has over 14 years of experience in global clinical development, leading Phase I–III trials across multiple therapeutic areas, with a particular focus on new drug development projects. She has extensive expertise in project leadership, study start-up, investigational product management, and global site/vendor communication. As a clinical team leader, she has directed cross-functional teams and contributed to IND submissions, ensuring successful execution of global clinical trials.

    Session Details:

    Managing Investigational Product (IP) in Clinical Trials: Best Practices for Compliance, Safety, and Efficiency

    2025-12-02, 4:15 PM

    Session Details:

    PANEL DISCUSSION: Stronger Together: Mastering Vendor Relationships for Game Changing Clinical Supply Results

    2025-12-02, 4:45 PM

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    Tina Sun
    Tina Sun, SSO, Country Head, Novartis (Taiwan); President, TCRA (Taiwan Clinical Research Association)

    With over 20 years of experience in clinical operations, Tina held leadership positions at Eli Lilly and Novartis, managing operations in Taiwan and Hong Kong. Besides her corporate roles, she led Transcelerate Taiwan since 2013 and served twice as the president of the Taiwan Clinical Research Association. Tina is interested in external engagement activities through her journey in clinical operations. Her authority in the field is demonstrated further through speaker roles at universities, conferences and clinical trial training programs, particularly on GCP-related topics.

    Specialties

    Global clinical trials operations and management

    Speaker of clinical trial topics in GCP training program, university and conference

    Professional Experiences

    Trial Monitoring Country Head, Novartis (Taiwan)

    Head of Clinical Operations, Eli Lilly and Company (Taiwan & Hong Kong)

    President of Taiwan Clinical Research Association (5th ,TCRA)

    Medical representative, clinical research associate, Novartis (Taiwan)

    Pharmacist, Po-Ai Hospital

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    Jung Won Jung
    Production Team Manager, inno.N

    Session Details:

    GMP and Global Trials: Managing Multi-Regional Requirements for Manufacturing and Labeling

    2025-12-02, 2:15 PM

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    Hyesung Shin
    Director, Clinical Development Strategy, R&D Division, Aptabio

    Hyesung Shin, managing director of TiumBio Co., Ltd has worked more than 23 years of experience in clinical trial development and operations.

    She had worked during 13 years for global pharmaceutical companies at Eli Lilly, Novo Nordisk and Novartis and 6 years at Abbott for medical devices clinical development and had experienced in Korean Biotech companies of BioPharm Solutions, Aptabio Therapeutics, TiumBio for new drug development and managing phase I/II Clinical Trial.

    The works focused on managing clinical trial plan for new drug development, regulatory Filing for FDA/EMEA/MFDS IND, orphan drug Designation, vender management including CRO/Clinical Supplies/CDMO and development of  market strategy.

    Session Details:

    Streamlining the End-to-End pharmaceutical supply Chain: Enhancing efficiency and quality

    2025-12-03, 10:00 AM

    Session Details:

    PANEL DISCUSSION: Turning Transit Troubles into Triumphs: Proven Strategies for Clinical Supply Success

    2025-12-03, 12:15 PM

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    Sangmi Lee
    Head of Clinical Development, ABL Bio

    A seasoned leader with over two decades of experience in clinical development, Sangmi Lee is currently the Head of Clinical Development at ABL Bio Inc., where she spearheads the company's oncology pipeline. Her extensive career spans both global and local pharmaceutical landscapes, including leadership roles at Novartis, Chong Kun Dang, and GreenCross.

    Specializing in early-stage development, Sangmi Lee has deep expertise in advancing complex therapeutic modalities, with a particular focus on T-cell engagers, bispecific antibodies, and bispecific ADCs. Her presentation, "Optimizing T Cell Engaging Therapies from Preclinical Study to Human Clinical Trial," will draw on her comprehensive background in translating cutting-edge science into successful human clinical trials.

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    Jeffery Wong
    Senior Director of Business Development, Nucleus Network

    Jeffery Wong is the Senior Director of Business Development at Nucleus Network, one of the world’s largest Phase I Clinical Trial Service provider with operations spreading across both Australia and the USA.

    A strong business development professional, Jeffery graduated from RMIT University, holds a Masters in Business and Biotechnology with a major in Pharmaceutical Sciences. During his 18 years with Nucleus Network, Jeffery has seen the growth of Nucleus Network from a 24 bed not for profit organisation to its current capacity of over 200 phase I beds spread across the globe.

    Jeffery has a passion in supporting industry members to achieve their clinical development goals and leverages on his extensive knowledge in business development, project operation, clinical study design and regulatory affairs.

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    Jessica (Youngji) Han
    Jessica (Youngji) Han, Director, Asian Operations, Avance Clinical
    Jessica (Youngji) Han has over 18 years of experience in the healthcare and clinical research industry, with strong expertise in clinical operations, project management, and regulatory strategy.
    At Avance Clinical, Jessica oversees the development of a robust operational platform across Asia, integrating clinical delivery excellence, regulatory expertise, and local partnerships. Her leadership ensures that biotech sponsors can conduct high-quality, efficient, and compliant clinical trials tailored to the unique dynamics of the APAC region.
    Avance Clinical has been instrumental in advancing its GlobalReady Pathway, which connects Australia’s early-phase ecosystem with Asia’s scalability — accelerating global drug development for innovative biotech companies.
    Jessica’s strategic focus and operational insight position Avance Clinical as a trusted partner for biotechs seeking to leverage Asia’s diverse patient populations and world-class research infrastructure to achieve their clinical development goals efficiently.
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    Derek Grimes
    EVP, Global Clinical Research, QPS Holdings, LLC

    Derek Grimes is the Executive Vice President of Global Clinical Research at QPS Holdings, LLC, where he leads global Phase I–IV clinical operations and strategic partnerships. With over two decades of experience in clinical research, Derek has built and managed large-scale programs across the US, Europe, and APAC, specializing in oncology and early-phase drug development. Before joining QPS, he held senior leadership roles in academic and industry settings, where he focused on operational excellence, innovation in clinical trial execution, and global regulatory strategy. Derek is passionate about bridging US and APAC clinical research ecosystems to accelerate global drug development.

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    Anna Park
    Industry Affairs Manager, International Air Transport Association (IATA)

    Anna Park is the Industry Affairs Manager at the International Air Transport Association (IATA). She is based at the country office of the Republic of Korea in Seoul.
    IATA is the trade association for the world’s airlines, representing some 300 airlines or 83% of total air traffic. IATA supports many areas of aviation activity and helps formulate industry policy on critical aviation issues. In her role, Anna looks after industry advocacy affairs, IATA’s product and service delivery to Air Cargo dedicated to certification, digitalization (One Record), and data solutions, as well as Customer Experience such as One ID initiative in the Korean market.
    A key focus of her portfolio is supporting member airlines and aviation stakeholders in promoting global standards and practical solutions that enhance air cargo operations such as CEIV Pharma certification and the implementation of IATA guidelines that strengthen quality and compliance across the cargo supply chain. Anna has enriched experience over 17 years in the aviation industry including a 9-year stint at their Asia-Pacific regional office in Singapore and has been with IATA since 2008

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    Heewon Lee
    Manager, Clinical Research Lead, Eli Lilly

    Heewon Lee is a Clinical Research Lead at Eli Lilly, responsible for leading the initiation and operation execution of clinical trials for Lilly molecules. Her work focuses on country feasibility, site selection, and investigator engagement. She has over 12 years of experience in the pharmaceutical industry brings deep expertise in clinical operations.

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    Chris Wallace
    Head of Distribution EMEA, Argenx

    Chris has over 35 years’ varied supply chain experience, having worked for several blue chip companies in a number of industries including 3rd party logistics services, automotive, medical device, nuclear fuels and biotech/pharmaceuticals.

    Originally from the UK but now based in Switzerland, he has been involved in life science - biotech/pharmaceuticals & medical device - for over 20 years of his career and has latterly been SVP Global Supply Chain at Clover Biopharmaceutical before last year moving to Argenx as Head of Distribution EMEA.

    He has developed, implemented and managed global healthcare supply chain strategies and operations on 6 continents. This has included different set-ups in multiple countries, including many in the Emerging Markets as well as the developed world.

    Chris has a degree in economics from Manchester University, an MBA from Aston University and a postgraduate diploma from London University. In his spare time, he plays golf badly and loves to sample great Italian food and red wines!

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    Luiz Barberini
    Head of External Manufacturing, Latin America, Bayer
    • Over 25 years’ experience in Logistics, Supply Chain, Procurement and Demand Planning areas.
      Solid knowledge and experience in the whole S&OP process and its KPI´s inter-relationships with stakeholders
    • Demand Planning process management - pre-S&OP, with Sales, Marketing, Trade Marketing, Industrial Planning and Finance and customized tool design for such process
    • Management skills: experience with multidisciplinary and international teams (Brazil / Latin America / US).
    • Experience in S&OP, 3PL and Supply Chain Organization projects' implementation
    • Strong experience with Pharmaceutical and Consumer companies and Brazilian distribution model / 3PL contracts
    • Solid team management skills, as well as Customer Service relationship and management
    • Teacher for major Post Graduation Schools - Demand Planning and Procurement/Negotiation areas

    CSCP & CPIM APICS. Logistics & Supply Chain driven strategy. Distribution & Logistics, Demand Planning, S&OP, Procurement and Export experiences, focusing on Business necessities through effective leadership.

    Working as External Manufacturing Operations Manager Latin America at Bayer, in charge for external partners for CHC Division. Previously as Relationship Associated Director at Merck , Logistics Manager at Takeda/Nycomed Pharma, focusing on demand management, planning and distribution activities. Also has worked as Pfizer´s Logistic Manager and EFD´s Supply Chain Manager. Souza Cruz´s Procurement Manager and Rhodia's Logistic Supervisor.

    Specialties: Logistics, Supply Chain, Materials, Procurement , Services, Negotiation, 3PL contracts, S&OP, Demand Planning

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    Amanda Briceno
    Clinical Supply Management & Patient Centricity Unit Manager, Chiesi Farmaceutici

    Amanda Briceno is an experienced clinical supply professional with over 10 years in clinical research and supply chain operations. Originally from Venezuela, now based in Italy. She currently serves as Clinical Supply Manager and Head of the Patient Centricity Unit at Chiesi Farmaceutici, where she leads initiatives to design and deliver patient-focused clinical supply solutions that improve trial compliance and enhance the experience of both patients and site staff.

    Her career began as a Clinical Research Associate at IQVIA, where she gained extensive experience in global trial monitoring and operations. Since joining Chiesi, Amanda has held positions of increasing responsibility within the Clinical Supply department, before assuming her current leadership role.

    Amanda holds a Master’s degree in Drug Biotechnology from the Università degli Studi di Milano and a Bachelor’s degree in Medical Biotechnology. Amanda brings a strong blend of technical knowledge and operational leadership. Passionate about innovation in clinical supplies, she is dedicated to advancing more accessible, patient-centric clinical trials.

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    Paul Hingst
    Supply Chain Consultant, Crinetics Pharmaceuticals

    Paul is an experienced Clinical Supply Chain Professional with a 25-year career in the BioPharmaceutical industry.  His extensive career includes roles at major companies like Amgen and Thermo Fisher Scientific, where he honed his skills and made a significant impact.  He has served in varied roles from basic research and contract manufacturing to client services and account management.  He is a Principal Consultant and Co-Founder of Beacon BioPharm Associates, a clinical supply chain consulting firm, providing variable staffing solutions to small and mid-sized BioPharm clients.  Paul is an industry veteran and respected leader known for his expertise in clinical supply chain.

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    Amaury Jeandrain
    Strategy Advisor, Clinical Supply, N-SIDE

    Amaury Jeandrain has a Master’s Degree in Business Engineering with a specialization in supply chain optimization. He joined Clinigen in 2015, then N-SIDE in 2016 where he last  held the position of VP of Strategy for clinical supply solutions.

    Over the past decade, his objective has been to make clinical trial supply chains more efficient by redefining CTS strategies and driving measurable performance improvements. His expertise also includes forecasting, planning, waste reduction, and shortage risk mitigation.

    Since 2024, while accompanying his wife on humanitarian missions abroad (Niger, then Colombia), Amaury has continued his work as a CTS advisor and trainer, partnering with pharmaceutical companies worldwide to enhance clinical supply performance.

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    Francesco Santo
    Director Clinical Supply Chain,
    Orano Med

    A highly experienced and passionate Director Clinical Supply Chain, Francesco has dedicated the past 17 years to ensuring the seamless execution of clinical trials by optimizing supply chain operations. His deep commitment to this field is driven by a relentless pursuit of excellence in delivering life-saving treatments to patients worldwide.  Throughout his career, he has honed a diverse skill set, encompassing:

    • Strategic Supply Chain Management
    • Regulatory Compliance
    • Cross-Functional Collaboration
    • Risk Management
    • Innovative Problem-Solving

    Francesco’s dedication to the clinical supplies industry is rooted in a profound understanding of the critical role it plays in advancing medical research and improving patient outcomes. He is committed to continuing his journey in this field, always striving to contribute to the betterment of global health.

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    Arnaud Dourlens
    Global Head of Clinical Supply Chain Operations, Sanofi

    Arnaud Dourlens is an Arts et Métiers engineer, he began his industrial career in the FMCG sector where he held growing responsibilities. Then he joined the LVMH group where he reorganized new product launches and industrial investments in the Make-up segment in order to adapt to the need for innovation and time to market, thus providing a competitive advantage. He then managed the entire portfolio of industrial launches and investments in Perfumes, Skincare and Make-up for Parfums Christian Dior Group.

    During his career Arnaud held a wide variety of industrial roles. He joined Sanofi in 2017 as Production Director of a major solid oral form production site (>2.5 billion € turnover). He has been a key player in the development of the continuous improvement mindset and in the transformation of the site through IT projects, investments and activity growth following the acquisition of Boehringer Ingelheim consumer healthcare portfolio.

    Since the beginning of 2020, he’s been the global head of Sanofi Clinical Supply Chain Operations, managing worldwide clinical supply teams involved in more than 300 clinical studies.

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    Paul Larochelle
    Senior Director Global Clinical Supply Chain,
    Takeda

    Paul Larochelle currently serves as Senior Director (Planning Team Lead) for Global Clinical Supply Chain at Takeda, where he serves as a member of the GCSC Leadership Team and is responsible for managing a team of professionals overseeing the forecasting and planning of clinical study supplies. His role encompasses the strategic and operational aspects of clinical supply chain management in therapeutic areas such as oncology, neuroscience, gastrointestinal diseases, vaccines, and rare diseases. Paul's leadership extends to cross-functional projects aimed at implementing new capabilities, conducting due diligence of potential acquisitions by the company, and improving existing processes.

    Previously, Paul held various roles at Biogen Corporation and Genzyme, a Sanofi Company, where he honed his expertise in clinical asset planning and clinical supplies management. His contributions to these organizations included serving as a lead contact for multiple clinical programs, developing supply chain strategies, leading continuous improvement projects, and serving as Fellowship Coordinator and Student Preceptor for dozens of students.

    Paul has a BS in Biology from Providence College, PharmD from MCPHS Boston, and an MBA from Worcester Polytechnic Institute. He also completed a Post-PharmD Industry Fellowship in Clinical Research/Investigational Product Management with MCPHS-Worcester and Genzyme Corporation. He is Chair of the Dean's Advisory Board at MCPHS School of Pharmacy – Boston,  a member of the Pharmacy Advisory Board at Western New England University, and a member of the Advisory Board for the Clinical Trial Supply global conference series.

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