Clinical Trial Supply China 2025 <br/>中国临床试验供应链大会2025

The Clinical Trial Supply China conference launch is your gateway to understanding and excelling in the rapidly evolving landscape of clinical trial logistics in China. </br> 中国临床试验供应链大会的召开，将为您提供深入理解并领跑中国临床试验物流快速变革格局的重要契机。

3 - 4

September

2025
  • Suzhou, China 中国，苏州
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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.

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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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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.

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

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Company Website

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

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The Almac Group is an established contract development and manufacturing organisation providing an extensive range of integrated services across the drug development lifecycle to the pharmaceutical and biotech sectors globally.

Its innovative services range from R&D, biomarker discovery development and commercialisation, API manufacture, formulation development, clinical trial supply, IRT (IVRS/IWRS) through to commercial-scale manufacture.

The international company is a privately owned organisation which has grown organically over the past five decades now employing over 5,600 highly skilled personnel across 18 facilities including Europe, the US and Asia.

The company has a global reputation for excellence built over 50 years of client service, delivering expertise right across the drug development lifecycle and offering a tailored solution to each of our clients.

To keep up to date with latest news, follow Almac Group on Twitter and LinkedIn or visit almacgroup.com.

Company Website

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

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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.

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

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Complex innovative clinical trial designs require an integrated synergetic approach to assess novel drug compounds for safety and effectiveness which often span esoteric, regulated and safety outcomes in all phases of the drug development life-cycle.

The companies of Eurofins BioPharma Services provide a seamless solutions-based approach in support of phase I to IV clinical trials with a unique analytical testing portfolio for Central Laboratory Services, Bioanalytical Services and complex Biomarker Assay Development and Testing Services for drug and vaccine development.

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

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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

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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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Company Website

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

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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.

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

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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?

    Why attend? 为何参会？

    The launch of  Outsourcing and Clinical Trials China is your opportunity to engage with the forefront of clinical trial innovation in one of the fastest-growing markets for clinical research. Here’s why you should attend:

    “中国临床试验外包大会” 为您提供与全球增长最快的临床研究市场创新前沿接轨的机遇。以下是您不容错过的理由：

    Access Local Expertise: Gain insights into the unique challenges and opportunities within China’s clinical trials landscape, directly from local and international experts.

    获取本土洞见
    直击中国临床试验生态的独特挑战与机遇，聆听中外专家的第一手经验分享。

     

    Regulatory Updates: Stay ahead with the latest regulatory developments and compliance strategies essential for navigating China’s evolving healthcare environment.

    掌握法规动态
    获取中国快速演变的医疗监管政策最新进展，学习合规策略以规避风险。

    Industry Networking: Build meaningful connections with leading CROs, biopharmaceutical companies, and other stakeholders driving clinical trial success in China.

    拓展行业人脉
    与推动中国临床试验成功的CRO龙头企业、生物制药公司及行业决策者建立深度合作。

    Strategic Collaboration: Explore strategies to optimize outsourcing partnerships and discover tailored solutions for managing clinical trial operations in a complex, dynamic market.

    优化合作战略
    探索复杂动态市场中的外包合作模式，定制化临床运营解决方案。

     

    Emerging Trends: Delve into cutting-edge technologies and methodologies shaping the future of clinical trials in China, from digital tools to innovative supply chain solutions.

    前瞻未来趋势
    聚焦数字化工具与创新供应链等前沿技术，洞察中国临床试验的未来形态。

     

    CTS

    Clinical Trial Supply China 2025

    The Clinical Trial Supply China conference launch is your gateway to understanding and excelling in the rapidly evolving landscape of clinical trial logistics in China.

    中国临床试验供应链大会2025
    中国临床试验供应链大会的召开，将为您提供深入理解并领跑中国临床试验物流快速变革格局的重要契机。

    Why attend?

    为何参会？

    The Clinical Trial Supply China conference launch is your gateway to understanding and excelling in the rapidly evolving landscape of clinical trial logistics in China. Here’s why you should join:

    “中国临床试验供应链大会”是您深入理解并驾驭中国临床试验物流快速变革格局的关键平台。以下是您不容错过的核心价值：

    Navigate Local Challenges: Gain critical insights into the unique complexities of clinical trial supply chains in China, including import/export regulations, regional distribution, and local manufacturing.

    破解本土化难题
    深度解析中国临床试验供应链特有的复杂挑战，包括进出口监管政策、区域配送网络布局及本土化生产策略等核心议题。

    Regulatory Expertise: Stay updated on China’s regulatory environment, ensuring compliance while minimizing delays and risks in your clinical trial supply processes.

    掌握监管先机
    实时获取中国药监动态，系统学习如何在确保合规前提下，规避供应链延误风险与质量隐患。

    Build Strategic Partnerships: Connect with key stakeholders, including suppliers, logistics providers, and biopharmaceutical companies, to foster collaborations that drive efficiency and innovation.

    缔造战略联盟
    与供应链核心决策者直接对话：包括头部物流服务商、本土供应商及跨国药企供应链负责人，构建高效协同网络。

    Discover Innovative Solutions: Explore cutting-edge tools, technologies, and strategies to optimize supply chain management, ensure product integrity, and reduce operational costs.

    解锁创新方案
    探索保障产品完整性的前沿技术：从智能温控物流系统到区块链追溯平台，获取降本增效的实战解决方案

    Stay Ahead of Trends: Learn about emerging trends and future directions in clinical trial supply tailored specifically to the Chinese market.

    洞见未来趋势
    聚焦中国市场独有的发展趋势：从MAH制度下的供应链重构到临床急需药物特殊通道，把握政策红利窗口期

    Whether you’re launching trials in China or looking to refine your supply chain operations, this conference provides the knowledge and connections you need to thrive in one of the most dynamic markets for clinical trials.

    无论您是首次在中国开展临床试验，还是寻求优化现有供应链体系，本次大会都将为您提供在这个最具活力的临床试验市场中蓬勃发展所需的关键洞见与战略人脉。

    Agenda

    • 3 Sep 2025
    • 4 Sep 2025
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    8 AM

    Registration and refreshments
    注册签到 & 茶歇交流

    8:30 AM

    Chairperson’s opening remarks
    主席开幕致辞

    8:45 AM

    Opening Keynote Panel
    开幕主题论坛

    The Evolving Clinical Trial Landscape in China: Challenges & Opportunities

    China has emerged as a key player in global clinical research, driven by regulatory reforms, a vast patient population, and increasing investments in biotechnology. This panel discussion will provide a comprehensive overview of the current clinical trial landscape in China, examining the challenges, opportunities, and future outlook for sponsors, CROs, and global stakeholders.

    • Current State of Clinical Trials in China; Growth trends and recent developments in the Chinese clinical trial ecosystem, impact of regulatory reforms, including NMPA’s efforts to streamline approvals, China’s role in global multi-regional clinical trials (MRCTs);
    • Challenges Facing Clinical Trials in China; Navigating regulatory complexities, Intellectual property (IP) concerns and data protection in clinical research, Operational challenges: site selection, patient recruitment, and investigator training, Differences in trial execution compared to the U.S. and EU
    • Clinical Trial Supply Chain: Challenges and Best Practice; Strategies for reducing supply chain disruptions and ensuring compliance
    • Opportunities for Sponsors & CROs
    • The Future of Clinical Trials in China; How China is positioning itself as a leader in global drug development. Potential impact of geopolitical factors on international collaboration

    中国临床试验格局的演变：挑战与机遇

    中国凭借监管改革、庞大的患者群体及对生物技术日益增长的投资，已成为全球临床研究的关键参与者。本论坛将全面剖析中国临床试验的现状，探讨申办方、CRO及全球利益相关方面临的挑战、机遇与未来前景。

    • 中国临床试验现状：中国临床试验生态系统的增长趋势与最新进展；监管改革的影响（包括NMPA审批流程优化举措）；中国在全球多区域临床试验（MRCT）中的角色
    • 中国临床试验面临的挑战：复杂监管环境的应对策略；知识产权保护与临床研究数据安全；实操难点：研究中心筛选、患者招募及研究者培训；中美欧临床试验执行的差异性分析
    • 临床试验供应链：挑战与最佳实践
    • 降低供应链中断风险与合规保障策略
    • 赞助商与CRO的机遇

    中国临床试验的未来图景：中国如何确立全球药物研发领导地位；地缘政治因素对国际合作的潜在影响

    9:30 AM

    Reserved for Event Sponsor
    赞助商专场

    10 AM

    Global Relationships: Enhancing Collaboration in Outsourcing
    全球合作：加强外包协作关系

    • Working with Chinese CROs and CMOs – what global sponsors should know
    • Managing cross-border clinical trials: logistics, communication, and cultural considerations
    • Case studies of successful global-China partnerships

     

    • 与全球CRO/CMO合作——中国企业必备指南
    • 跨国临床试验管理要点：物流协调、沟通机制与文化适配
    • 中外合作成功案例深度解析

    10:30 AM

    Reserved for Event Sponsor
    赞助商专场

    11 AM

    Morning refreshments and networking – Please visit 3 booths in this break
    上午茶歇与交流互动——请在此期间至少参观3个展位

    11:30 AM

    Overview of the clinical trial supply landscape in China
    中国临床试验供应链全景透视

    • The growing role of China in global clinical trials
    • Key challenges facing clinical trial supply chains in China: logistics, regulations, and patient populations

     

    • 中国在全球临床试验中日益凸显的核心地位
      • 供应链三大核心挑战：
    • 跨境物流与本土配送体系
    • 动态监管合规要求
    • 特殊患者群体的供应保障

    12 PM

    Reserved for event Sponsor
    冷链与温控物流管理

    Cold Chain and Temperature-Controlled Logistics

    • Ensuring the integrity of temperature- sensitive products: Managing biologics, vaccines, and other temperature- sensitive investigational drugs
    • Challenges in cold chain logistics in China: Long distances, varied climates, and infrastructure limitations
    • Solutions for temperature-controlled packaging, transport, and storage
    • Real-time temperature monitoring systems for cold chain compliance
    • Case study: Successful cold chain management for a multi-center trial in China

     

    • 保障温度敏感型产品完整性：生物制剂、疫苗及其他温度敏感型试验用药的管理
    • 中国冷链物流的特殊挑战：长距离运输、多样化气候条件及基础设施限制
    • 温控包装、运输与储存解决方案
    • 实时温度监控系统在冷链合规中的应用
    • 案例研究：中国多中心试验中的成功冷链管理实践

    1 PM

    Lunch and networking – Please visit 3 booths in this break
    午餐交流时间——请在此期间参观至少3个展位

    2:15 PM

    Selecting and Fostering Vendor Relationships
    供应商选择与合作关系培育

    • Choosing the right vendors: Best practices for selecting CMOs (Contract Manufacturing Organizations), logistics providers, and technology suppliers
    • Building and maintaining strong vendor relationships: How to foster long-term, collaborative partnerships in China
    • Criteria for evaluating vendor capabilities in compliance, quality, and local expertise
    • Navigating vendor selection challenges in China for clinical trial supply

     

    • 优选供应商策略：CMO（合同生产组织）、物流服务商与技术供应商的遴选标准
    • 建立可持续的合作关系：中国本土长期协作伙伴培养之道
    • 供应商能力评估维度：合规性、质量体系与本地化专业能力
    • 中国临床试验供应链供应商选择的特殊挑战

    2:45 PM

    Reserved for event Sponsor
    赞助商专场

    3:15 PM

    Innovation and Technology for Supply Chain Efficiency
    创新技术提升供应链效率

    • Technology-driven solutions for optimizing clinical trial supply chains
    • Artificial Intelligence (AI) and Machine Learning (ML): Forecasting demand,
    • optimizing inventory management, and improving logistics
    • Enhancing data integrity and traceability
    • E-labelling: The future of digital labelling solutions for investigational products

     

    • 技术驱动的临床试验供应链优化方案
    • 人工智能（AI）与机器学习（ML）：需求预测、库存管理优化和物流改进
    • 提升数据完整性与可追溯性
    • 电子标签（E-labelling）：试验用药品数字标签解决方案的未来趋势

    3:45 PM

    Afternoon refreshments and networking – Please visit 3 booths in this break
    下午茶歇与交流时间——请在此期间参观至少3个展位

    4:30 PM

    Risk Management and Forecasting
    风险管理与需求预测

    • Forecasting and planning: Using predictive analytics for accurate demand forecasting and minimizing supply shortages
    • Risk management strategies: Identifying and mitigating risks
    • Building contingency plans to address disruptions in the supply chain, from production delays to shipping issues
    • Direct-to-patient shipping: Managing risks and benefits of shipping clinical trial products directly to patients in remote areas

     

    • 预测分析技术应用：精准需求预测与供应短缺预防
    • 风险管理机制：关键风险识别与应对方案
    • 供应链中断应急预案（涵盖生产延误至运输问题全场景）
    • 直达患者配送模式：偏远地区临床试验产品直送的风险收益评估

    5 PM

    PANEL DISCUSSION: Optimising Clinical Trial Supply in China
    专题讨论：中国临床试验供应链优化之道

    • Cold chain and temperature-controlled logistics management
    • Compliance with NMPA and international shipping regulations
    • Innovations in AI, ML, and real-time supply chain monitoring
    • Vendor relationship management and forecasting in China

     

    •  冷链及温控物流管理
    • 符合NMPA与国际运输法规的合规实践
    • AI、机器学习与实时供应链监控技术创新
    • 中国本土供应商关系管理与需求预测
    • 观众公开问答环节

    5:30 PM

    Chairperson’s closing remarks
    大会主席总结致辞

    8:30 AM

    Registration and refreshments
    注册签到与茶歇交流

    9:10 AM

    Chairperson’s opening remarks
    主席开幕致辞

    9:15 AM

    Comparator and Placebo Sourcing
    对照药与安慰剂供应解决方案

    • Sourcing comparators and placebos in China: Ensuring supply, regulatory compliance, and cost-effectiveness
    • Addressing supply chain challenges specific to comparator and placebo sourcing
    • Partnering with local vendors for sourcing in compliance with regulatory standards
    • Efficiently managing comparator sourcing in a multi-country trial

     

    • 中国本土供应体系构建：确保可及性、合规性与成本效益
    • 对照药供应链特殊挑战应对方案
    • 符合监管标准的本土供应商合作机制
    • 跨国多中心试验中的高效供应管理

    9:45 AM

    Reserved for Event Sponsor
    赞助商专场

    10:15 AM

    Streamlining end-to-end pharmaceutical supply Chain: enhancing efficiency and quality
    端到端药品供应链优化：效能与质量双提升

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

     

    • 从生产到患者交付的全链路挑战解析
    • 动态监管合规要求应对方案
    • 供应链效能提升实施路径

    10:45 AM

    Morning refreshments and networking – Please visit 3 booths in this break
    上午茶歇与交流互动——请在此期间至少参观3个展位

    11:45 AM

    Reserved for Event Sponsor
    赞助商专场

    12:15 PM

    PANEL DISCUSSION Tackling delays in clinical supply: Strategies and Solutions
    专题讨论

    • Strategies to minimize delays in clinical supply Logistics
    • Implementing effective communication through ‘Huddles’
    • Practical Solutions for Streamlining Supply Chain Processes

     

    破解临床供应链延迟难题：策略与解决方案

    • 临床供应链物流延迟最小化方案
    • 通过"短频快"沟通机制提升协同效率
    • 供应链流程优化实战案例解析

    1 PM

    Lunch and networking – Please visit 3 booths in this break
    午餐交流时间——请在此期间参观至少3个展位

    2:30 PM

    PANEL The Rise of Chinese Biotech: a competitive challenge for U.S. companies and investors
    专题讨论

    China’s biotech industry has rapidly expanded, posing increasing competition to U.S. biotech firms in drug development, clinical trials, and global market entry. With strong government support, access to capital, and a growing pipeline of innovative therapies, Chinese biotech companies— backed by aggressive venture capital (VC) funding—are reshaping the industry. This session will analyse the competitive landscape, the challenges faced by U.S. biotech firms, and the future dynamics of global biotech innovation.

    • The Rise of China’s Biotech Industry: The Chinese government’s “Made in China 2025” strategy and its impact on biotech innovation
    • The role of China’s National Medical Products Administration (NMPA) in accelerating drug approvals
    • The Role of Venture Capital in China’s Biotech Boom; How Chinese VCs and state-backed funds are fueling biotech startups and the differences between U.S. and Chinese biotech funding models
    • Competitive Pressure on U.S. Biotech Firms
    • Regulatory & Geopolitical Challenges: The impact of U.S.-China trade tensions and export controls on biotech collaboration

    中国生物科技崛起：美国企业与投资者的竞争挑战

    中国生物科技产业迅猛发展，在药物研发、临床试验及全球市场拓展方面对美国生物科技企业构成日益激烈的竞争。凭借政府强力支持、资本优势及创新疗法管线的持续扩充，在风险投资（VC）加持下的中国生物科技企业正在重塑行业格局。本环节将深入分析竞争态势、美国企业面临的挑战以及全球生物科技创新的未来走向。

    • 中国生物科技产业崛起："中国制造2025"战略对生物科技创新的推动效应
    • 监管加速作用：中国国家药品监督管理局（NMPA）在新药审批中的角色演进
    • 资本驱动力量：中美国际资本运作模式差异——中国风险投资与政府基金如何赋能生物科技初创企业
    • 美国企业的竞争压力：核心技术与市场份额的双重挑战
    • 监管与地缘政治因素：中美贸易摩擦及出口管制对生物科技合作的影响

    3:15 PM

    Speaker Hosted Roundtables
    嘉宾主持圆桌讨论会

    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: What key aspects of inspection readiness should be considered right now?
    ROUNDTABLE 2: Getting the best out of your sponsor – CRO partnership
    ROUNDTABLE 3: Ensuring clinical quality assurance in supply chain management

     

    互动式圆桌会议为您提供与同行深入交流的独特机会，共同探讨行业关键挑战的解决方案并分享最佳实践。每场讨论由行业专家主持，聚焦单一议题，通过高互动形式拓展人脉网络，汲取他人经验智慧。
    （每场圆桌讨论时长30分钟，参会者可轮换参与）

    圆桌议题1：当前核查准备工作的核心要素
    圆桌议题2：如何构建最优申办方-CRO合作伙伴关系
    圆桌议题3：临床试验供应链质量管理保障机制

    4:15 PM

    Chairperson’s closing remarks and Prize Draw Join us for a chance to win one of our prizes, including Technology products
    大会总结致辞与抽奖环节 参与即有机会赢取科技产品等丰厚奖品

    END OF CONFERENCE
    会议圆满结束

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    Partnership Opportunities

    We work with you to design a bespoke package to meet your business needs, where you could:

    • Demonstrate your expertise on the agenda – have the attention of the entire audience. For greatest impact, why not position your talk before a networking break and immediately conduct follow up conversations with highly engaged attendees
    • Showcase your business and its services at an exhibition booth, which provides a perfect meeting place for prospective new clients
      Present the value proposition of your offering over your competitors, in front of an audience of active, engaged potential customers
    • Speak with key decision makers as part of our intimate, interactive roundtable style workshop sessions with over 8 hours allowed for networking

    Event reach

    • 150+ attendees each year
    • 80% attendees C-suite level

     

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    SPONSORSHIP ENQUIRIES

    Jarvinder Sidhu

    Senior Sales Executive

    +44 207947 2755

    SPEAKER ENQUIRIES

    Maya Hudson

    Head of Production

    MARKETING ENQUIRIES

    Moona Popal

    Senior Marketing Manager

    DELEGATE ENQUIRIES

    Sunny Saikia

    VIP Delegate Manager

    Sponsorship Enquiries

     

    Jarvinder Sidhu

    Senior Sales Executive


    +44 207947 2755

    Speaker Enquiries

     

    Maya Hudson

    Deputy Head of Production


    +44 204540 7766