Highlights of the Conference

The PBCV – Clinical Trials Conference, taking place on April 23-24, 2026, at Shanghai, China, promises a dynamic and enriching experience for all attendees. This comprehensive program will focus on the latest advancements, technologies, regulations, and trends in clinical research, drug development, data innovation, and global health collaboration. Below are the key highlights of the conference:

Keynote Addresses by Global Clinical Research Leaders

Renowned clinical trial experts, regulatory authorities, industry leaders, and academic pioneers will deliver keynote addresses offering deep insights into trial innovation, regulatory science, patient-centricity, and the future of drug and device development.

Gain inspiration and strategic knowledge from thought leaders who are transforming clinical trials and global health research.

Cutting-Edge Research Presentations

Presentations from leading researchers and professionals will cover a wide range of topics including adaptive trial design, decentralized clinical trials (DCTs), AI in research, patient engagement strategies, real-world evidence (RWE), and therapeutic innovations.

Engage with high-impact research addressing critical challenges in trial design, efficiency, compliance, and health outcomes.

Panel Discussions on Challenges and Innovations in Clinical Trials

Panels will address timely issues such as regulatory harmonization, trial participant diversity, ethics in AI deployment, global trial feasibility, data transparency, and post-pandemic trial evolution.

Join these thought-provoking dialogues to explore cross-sector solutions and build forward-looking strategies for trial innovation.

Poster Sessions and Rising Researcher Awards

Poster sessions will spotlight contributions from early-career researchers, graduate students, and emerging professionals. Awards will be presented for outstanding posters based on innovation, methodology, and relevance to current clinical challenges.

Celebrate the next generation of clinical researchers and their contributions to improving public health through data-driven science.

Showcase of Innovations and Best Practices in Clinical Research

Explore case studies and real-world applications showcasing innovations like ePRO/eCOA, wearables, remote monitoring, AI-assisted trial design, and blockchain-enabled data verification.

Learn how these technologies are reshaping how trials are designed, monitored, and evaluated to increase speed, quality, and accessibility.

Networking Opportunities and Social Events

Connect with clinical operations professionals, sponsors, CROs, regulators, and academic leaders through structured networking sessions, receptions, and informal gatherings in the iconic city of Venice.

Build strategic partnerships, mentorship connections, and collaborative initiatives that extend far beyond the conference.

Roundtable Discussions and Special Interest Groups

Participate in in-depth sessions on specialized topics such as pediatric and rare disease trials, oncology, patient recruitment, site activation, regulatory affairs, and clinical data science.

Contribute to targeted discussions and engage with peers and experts who share your research focus or operational challenges.

Innovation and Technology Showcases

Engage with cutting-edge solutions in trial technology, including AI-powered platforms, mobile health applications, data interoperability systems, and remote trial infrastructure.

Meet the innovators driving efficiency, compliance, and participant-centricity in the clinical trials ecosystem.

Policy and Regulatory Updates

Sessions led by representatives from regulatory agencies and policy institutions will cover evolving trial guidelines, GCP updates, EMA/FDA regulatory frameworks, and ethical compliance trends.

Stay ahead of policy shifts and understand how global regulations impact your trial strategy and operations.

Global Perspectives and International Collaboration

International speakers will share insights on running trials across borders, addressing health inequities, overcoming logistical challenges, and ensuring cultural sensitivity in participant engagement.

Explore successful global collaborations and models that promote access, scalability, and sustainability in clinical research.

Ethics, Advocacy, and Sustainability in Clinical Trials

Sessions will focus on ethical challenges such as informed consent, AI transparency, patient advocacy, and data ownership. Discussions will also address sustainability in trial operations and long-term impact.

Learn how to apply ethical, inclusive, and sustainable frameworks to your clinical research practice and trial management.

Future Trends and Advancements in Clinical Research

Dive into the future of clinical trials, with sessions on precision medicine, genomics, hybrid models, digital biomarkers, patient-led research, and novel endpoints.

Understand where the field is headed and how you can lead change in a rapidly evolving research environment.

Abstract Publication and DOI Assignment

All accepted abstracts will be published in the official conference proceedings with Digital Object Identifier (DOI) assignment via Crossref, ensuring maximum academic exposure and citation potential.

The PBCV – Clinical Trials Conference is a must-attend event for anyone involved in clinical research and development. Whether you're a sponsor, investigator, CRO professional, data scientist, or policy expert, this event will deepen your knowledge, expand your network, and inspire innovation.

Join us in Shanghai, China, for a transformative global gathering committed to advancing excellence, equity, and innovation in clinical trials and research.