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April 23-24, 2026

8:00AM - 6:00PM

Shanghai
China

About Conference

PBCV – Clinical Trials Conference is a premier international event that brings together global leaders in clinical research, regulatory affairs, pharmaceutical development, academic medicine, and healthcare innovation. This high-impact gathering fosters collaboration and knowledge exchange on the latest advancements in clinical trials, drug development, patient safety, and evidence-based medical practices. Our mission is to provide a dynamic platform for critical dialogue and the dissemination of pioneering research that will shape the future of clinical research and healthcare delivery.

We are delighted to invite you to this prestigious conference dedicated to advancing excellence and innovation in clinical trials, scheduled for April 23-24, 2026, at the Shanghai, China. Join us for an immersive experience where scientific rigor meets regulatory strategy and patient-focused outcomes, creating an environment of global collaboration among researchers, sponsors, clinicians, policymakers, and industry professionals.

Theme of the Conference: Redefining Clinical Trials: Innovation, Ethics, and Global Collaboration in Medical Research

The PBCV – Clinical Trials Conference addresses key aspects of improving the design, conduct, regulation, and impact of clinical research globally. The agenda is shaped by the latest trends in digital health, decentralized trials, data integrity, and patient-centered research. Core focus areas include:

  • Clinical Trial Design and Methodology
  • Innovations in Drug and Device Development
  • Patient Recruitment, Engagement, and Retention
  • Regulatory Science and Global Harmonization
  • Real-World Evidence and Post-Market Surveillance
  • Decentralized and Virtual Trials
  • Clinical Data Management and Statistical Analysis
  • Ethics and Informed Consent in Research
  • Biomarkers and Personalized Medicine
  • AI, Big Data, and Digital Tools in Clinical Research
  • Risk-Based Monitoring and Quality Assurance
  • Pharmacovigilance and Safety Reporting
  • Diversity, Equity, and Inclusion in Clinical Trials

These topics reflect the rapidly evolving landscape of clinical research, highlighting transformative technologies, regulatory changes, and patient-centric models.

Key Features of the Conference:

Innovative Research Presentations:

Engage with groundbreaking studies and emerging technologies shaping the future of clinical trials—from AI-driven analytics to novel therapeutic approaches.

Expert-Led Panel Discussions:

Join leading voices from academia, regulatory bodies, pharma, and CROs in interactive panels tackling pressing issues like regulatory adaptation, trial transparency, and global trial expansion.

Strategic Networking Opportunities:

Forge connections with international experts and collaborators through curated networking sessions, roundtable discussions, and a dedicated exhibition space.

Poster Presentations and Exhibitions:

Present your clinical research findings, methodologies, or trial outcomes to a global audience. Poster sessions provide a valuable platform for feedback and interdisciplinary collaboration.

Global Insights and Best Practices:

Gain perspective on conducting trials in diverse regulatory environments and healthcare systems, promoting scalable solutions and global harmonization.

As clinical research enters a new era of innovation, regulatory transformation, and patient empowerment, professionals involved in clinical trials play a pivotal role in ensuring the development of safe, effective, and accessible therapies.

The PBCV – Clinical Trials Conference highlights the importance of robust methodology, ethical conduct, data transparency, and interdisciplinary collaboration in advancing medical science and improving health outcomes.

Who Should Attend:

  • Clinical Researchers and Principal Investigators
  • Regulatory Affairs and Compliance Professionals
  • Pharmaceutical and Biotech Executives
  • Contract Research Organizations (CROs)
  • Data Scientists and Biostatisticians
  • Medical and Scientific Affairs Teams
  • Research Coordinators and Study Nurses
  • IRB/IEC Members and Ethics Committee Representatives
  • Clinical Trial Managers and Monitors
  • Health Policy Experts and Advocates
  • Digital Health and AI Researchers
  • Academic and Industry Collaborators
  • Students and Early-Career Scientists in Clinical Research

Global collaboration in clinical research drives innovation, accelerates access to new therapies, and ensures ethical, evidence-based medical progress. The PBCV – Clinical Trials Conference is your opportunity to be part of this transformative journey.

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