Clinical trial professionals with an interest or role in the onboarding and education of new staff can learn valuable best practices from the steps taken, barriers encountered, and resources available during one clinical trial site’s journey toward realizing its goal for optimal efficiency.
This program explored medical devices and investigational medical devices.
This informative session explores some of the tools of the clinical research trade including data extraction and adverse event reporting.
This webinar highlighted best practices in various areas of clinical research management of investigator-initiated trials (IITs) and detailed how to navigate common challenges. The information included in this comprehensive review of IIT operations is experience-based and built upon good clinical research practices in alignment with NIH Regulations.
Gain the foundational knowledge clinical research professionals need to implement digital health components in clinical trials.