On-Demand Webinars
-
Balancing Data, Technology, And Strategy In Clinical Research
6/11/2024
Here, viewers will learn about best practices for developing an effective data collection strategy and selecting technology solutions that align with research needs.
-
Unleash The Power Of IQVIA Complete Consent
11/12/2024
Join Vinita Navadgi, and Amy Koller from IQVIA Complete Consent for an in-depth exploration of the eConsent landscape.
-
RTSM Considerations For Master Protocol Oncology Studies
1/20/2022
This webinar discusses the types of master protocols and how configurable, modern RTSM systems enable fast and seamless mid-study changes to help you efficiently run your master protocol study.
-
Site-Centric Clinical Platforms Are Better For Sponsors
Discover how seven of the top 15 global biopharmaceutical companies came together on a single clinical technology platform and operated through common workflows and common trial documents.
-
The Present And Future Of Study Supply Management
6/17/2024
Gain expert insights on the future of RTSM strategy and its evolution with the changing clinical supply and technology landscape in our webinar.
-
Improving Supply Chain: Accountability, Sustainability, Optimization
Watch as industry experts explore the advancements in drug accountability facilitated through IRT, encompassing innovative methods for managing site variations and sustainable supply chains.
-
Accelerating DHT Research And Drug Development
12/19/2024
This presentation focuses on the scope and utility of the National Health and Nutrition Examination Survey, a program of studies designed to assess the health status of individuals in the United States.
-
Reduce TMF Misfiles & Metadata Errors With Next-Gen AI-Enabled eTMF
4/17/2023
Listen in as Chief Product Officer Jim Nichols, Product Manager Jim Horstmann, and VP Solutions Consulting Aaron Grant discuss issues and solutions for trial master files.
-
De-Risking Clinical Trials: How A CTMS Can Help Adopt The ICH E6(R2)
6/20/2022
Explore how CTMS capabilities can help uncover hidden study risks with industry-standard questions in the CTMS library, score study risk based on likelihood, impact, and detectability, and manage key risk indicators.
-
Optimizing Efficiency And Quality In EDC Implementation
3/21/2023
Grant Williamson and Siba Noolu discuss best practices for ensuring quality and speed across EDC platforms for clinical operations, data management, and programming professionals.