The Global Clinical Trials Connect Conference is a premier platform bringing together global leaders, clinical researchers, regulatory experts, and technology pioneers to discuss the latest innovations, best practices, and challenges in clinical trials. This conference fosters collaborations between industry stakeholders to enhance trial efficiency, regulatory compliance, patient safety, and technological adoption.
This event unites experts across the clinical trial ecosystem to drive meaningful conversations on digital transformation, decentralized trials, regulatory pathways, patient engagement, and data-driven insights that are shaping the next era of clinical research
From adaptive trial designs to AI-powered analytics, this conference explores the latest trends, breakthrough technologies, and regulatory frameworks that are driving faster, more efficient, and more patient-centric clinical trials.
Clinical trials are no longer just about drug development, they are about people. A patient-first approach improves accessibility, engagement, and trial success. By leveraging digital advancements and innovative methodologies, research is becoming more inclusive and impactful.
At Business, we bring together brightest minds, leaders, and trailblazers from across industries to explore latest trends, technologies, and strategies shaping the future. Connect with professionals, decision-makers, and innovators from across the sector to expand your network and build lasting relationships. Gain valuable insights from thought leaders as they share strategies, real-world experiences, and forward-thinking perspectives. Explore the latest trends, tools, and technologies transforming the landscape and driving future growth.
Key highlights:
Global Regulatory Intelligence & Harmonization
Patient-Centric Trials & DE&I Strategies
Patient Recruitment, Retention & Site Selection
Site & Investigator Challenges, Enablement & Training
Decentralized & Hybrid Clinical Trials
Digital Health, Remote Monitoring & Wearables
Electronic Data Capture (EDC), eCOA, ePRO & e-Consent Solutions
AI, Big Data & Machine Learning in Clinical Trials
Clinical Data Quality, Strategy & Advanced Analytics
Real-World Evidence (RWE) & Real-World Data (RWD) Integration
Adaptive Trial Designs & Future-Proofing Operations
Clinical Technology, IRT & Automation Innovation
Blockchain & Cybersecurity in Clinical Research
Stakeholder Collaboration & Outsourcing Strategies
Regulatory Compliance, Risk-Based Monitoring & Clinical Auditing
Pharmacovigilance & Post-Trial Patient Engagement
Real-World Clinical Trial Strategies & Post-Market Safety Monitoring
Cost Optimization, Streamlined R&D & Trial Sustainability
Attendees includes VPs, GMs, Directors, Heads and Managers of
Clinical Trials & Clinical Study Management
Clinical Operations & Clinical Research Professionals
Patient Organizations & Patient Recruitment Specialists
Outsourcing & Vendor Management Teams
Site Management & Site Monitoring Experts
Clinical Pharmacology & Drug Development Experts
Clinical Data Management & Risk-Based Monitoring Experts
Clinical Research Sites, CROs, and CMOs
Hospitals, Research Institutes & Industry Associations
Regulatory Affairs & Compliance Professionals
AI & Data Science Experts in Clinical Trials
Real-World Evidence (RWE) & Big Data Analysts
Blockchain & Cybersecurity Professionals
Clinical Design, Protocol Strategy & Decision-Makers
Electronic Data Capture (EDC) & Digital Innovation Teams
Wearable & Digital Health Technology Developers
Biomarker & Precision Medicine Specialists
Supply Chain & Logistics Experts in Clinical Trials
Medical Affairs & Pharmacovigilance Professionals
Ethics Committees & Institutional Review Boards (IRBs)
Investors & Venture Capitalists in Clinical Research
