Accelerating clinical trial timelines, managing costs, and faster time to patient is the holy grail of clinical research. Join Ken Getz, Research Professor, Tufts University School of Medicine, for our opening keynote that explores the state of clinical trials today and the impact of technology solutions on the clinical trial operating enviroment.
Collaborating with external partners is crucial in the biopharmaceutical industry and can create challenges in managing data, maintaining security, and complying with regulations. Dr. Rebecca Carazza will share how Nimbus Therapeutics leveraged data governance as a foundation to collaborate with its partners and maintain data integrity in working across its partner network.
Robust security, compliance, and governance controls are critical to scaling and simplifying modern clinical data platforms. Join Jon Weiss on an insightful journey on how Egnyte can provide a cloud-native multilingual platform to enable a cutting-edge approach to statistical analysis of clinical data.
Data governance is vital in the life sciences industry, particularly concerning Electronic Document Management Systems (EDMS), Electronic Trial Master File (eTMF), Clinical Study Reports, and Statistics. Without standardized governance practices, we risk amplifying disorganized and unreliable data. Join Karen Travers and Mike Lynch, Halloran experts, as they share their experience of how governance frameworks are essential for maintaining data integrity and regulatory compliance across the clinical development lifecycle.
AI is a hot topic in biotech, but how much is real and how much is fantasy? Join experts from Digitalis Ventures, Alnylam Pharmaceutical and Luminaries Forge as they discuss how AI is changing Clinical Research today and how to prepare for tomorrow.
Join several of our speakers and Egnyte’s Life Sciences Leaders as they respond to audience questions, trends in the industry and future innovation.