Archives: Resources
The Strategic Advantage of Conducting Trials in Australia
Discover the benefits of early-phase trials in Australia.
Harnessing Generative AI for Clinical Trial Documentation
Explore the role of medical writers in ensuring the precision, accuracy, and regulatory compliance of AI-assisted documentation.
Beyond Numbers: The Value of In-Trial Interview Data for Regulatory and Health Technology Assessment (HTA) Decision-Making
A webinar exploring the added value of in-trial interview data in drug development and its pivotal role as a driver in decision-making for regulatory and HTA decisions.
Emerging global trends and regulatory hurdles in cell therapies for cancer
Watch our webinar to learn about emerging trends, commercialization hurdles, and regulatory actions in cell-based I-O therapies for cancer treatment.
Embracing a new CDMO and CRO partnership approach
Watch our webinar to discover how streamlining drug substances, products, and clinical research services can boost efficiency, cut timelines, and deliver therapies faster.
Three Transformative Strategies to Accelerate Clinical Trials in The Modern World
Watch this webinar to learn about key transformative strategies to accelerate trials in the modern world.
Humanizing patient recruitments in clinical research
Explore how to humanize patient recruitment in clinical research by focusing on patient education, AI and a patient-first approach.
Global Pharma R&D Insights
Our panel of experts highlights findings from our pharma R&D report and goes beyond the data to explain what these trends mean for drug developers across the globe.
Accelerating Drug Development through the Convergence of Real-World Data
Watch a panel discussion from DIA Global 2024 to explore how technology is reshaping clinical research and drug discovery.