Archives: Agenda

• Clinical contracting is on the critical path to trial start
• It is a process where bottlenecks and root causes can be identified via data analysis
• Lean Six Sigma methodology can help to significantly reduce contracting lead-time

• Operational inefficiencies quietly erode a drug’s Probability of Technical and Regulatory Success (PTRS) and reduce overall asset value
• Biotechs must shift from reactive oversight to proactive strategies grounded in near-term visibility and actionable data
• Same-day insights into trial conduct help de-risk execution, protect endpoints, and accelerate development timelines
• Faster, cleaner data drives confident decisions and signals operational strength to investors and partners
• Lessons from 25+ years in drug development offer a practical blueprint for embedding operation excellence into biotech strategy

Visit our exhibitors’ booths throughout the conference and collect stamps in order to enter our Prize Draw and be in for a chance of winning Apple devices or Amazon vouchers. The Prize Draw will take place in the Exhibition Hall, make sure you don’t miss out!

• Learn how to pressure-test site footprint through predictive analytics by forecasting enrollment at the country and site level
• Discover methods to run re-forecasts based on actual study performance for more accurate tracking and adjustments as necessary
• Gain competitive advantage thru actionable insights to remain agile and avoid costly enrollment delays
• Learn how to leverage data to identify low-performing sites earlier in the trial process to implement effective risk mitigation tactics

• The UAE as a prominent hub for research and clinical trials, driven by a focus on healthcare innovation and patient-centric approaches
• The UAE’s comprehensive regulatory framework that supports and facilitates clinical research
• Training and upskilling local researchers and clinicians in research methodologies
• Prioritizing patient-centric approach, engaging patient communities and advocacy groups

• Explore how PSI integrates GenAI for protocol similarity searches and enrollment rate predictions, improving accuracy and efficiency in clinical trial planning
• Learn how VISIONAL™ incorporates three new data sources to enhance site performance analysis and offer insights across 56 countries, supporting better decision-making
• Discover how VISIONAL™ enables sponsors to quickly generate multi-country feasibility scenarios and budgets in under 30 minutes, streamlining the planning process

• The challenge: Disconnected systems creating blind spots in trial management
• The opportunity: AI as the connective tissue between documentation and execution
• The Intelligent Trial Assistant: Natural Language Queries Across ETMF and CTMS
• AI-Driven Inspection Readiness: Connecting Document Quality to Trial Execution
• Predictive Trial Health: Using AI to Connect the Dots Between Documents and Operations
• Smart Document Classification Meets Smart Workflow: End-to-End Trial Automation