01.22.25 -- STREAM Edition: Adopting DCT's And Utilizing Mobile Research Nurses

Check out this workshop introduction to TrialKit AI’s dynamic analytics and reporting capabilities.

Compliance is more important than ever. Keep up with how regions are enforcing disclosure requirements by learning how to adjust compliance strategies accordingly.

Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.

Learn about a dedicated team delivering clinical development solutions for biotech and emerging biopharma customers. IQVIA Biotech is the CRO partner of choice for biotech companies around the world.

Vice President of Business Development Lisa Sanford explains whether you need an IND before starting your first-in-human trial in Canada.

Walk through how to manage and resolve the often conflicting internal and external directives to find the right path for you.

The need for remote access during the COVID-19 pandemic changed how clinical trials are conducted today. Yet there is still some uncertainty around which technologies to implement, the level of on-site versus virtual activities, and necessary operational changes.

Listen in as subject matter experts discuss three key components of a successful patient convenience strategy.

Explore the latest advancements in photoplethysmography (PPG) technology and discover how innovative cardiac metrics can enhance your research by joining the Q&A session with industry experts.

Dr. Steven Cummings highlights the role of PCM Trials certified mobile research nurses in making possible large-scale home-based clinical trial.