During their recent webinar on best practices for maintaining ethical and compliant delegation of authority (DOA) at research institutions, presenters Wendy Tate and Mariette Marsh discussed methods and tools to adequately navigate oversight of research operations in an increasingly complex clinical trial landscape. The two presenters received many attendee questions regarding the completion and maintenance…
Use these tips to streamline training workflows for protocol staff at your organization.
Medical coding dictionaries standardizes data interpretation, which increases data quality and minimizes risk.
CTMS-EMR integrations can provide significant benefits to research organizations, but it’s important to ensure that you’re leveraging the strengths of each system.
This Fall, over 200 clinical research professionals will attend the Onsemble Conference in Madison, WI. Here are five reasons you shouldn’t miss it.
Learn methods for addressing some of the research industry’s most pressing challenges and gain insights about performance metrics, effort tracking and more.
Stuart Cotter of Forte details what key issues a research institution can address by implementing an eRegulatory system.
How varying protocols and operations should change your organization’s approach to handling external data in your EDC system.
Integrating your clinical trial management system and electronic medical record can improve your workflows, patient safety and more.
Shopping for a validated EDC system can seem like a daunting task. Learn five steps that make the process less confusing.