Creating processes that result in accurate, timely and complete data are invaluable when implementing or optimizing a CTMS. Here are a few tips to achieve your goals.
Learn how centralized data can help institutions efficiently and accurately report their research performance and discover the tools to help.
Webinar presenter responds to these questions and provides resources for additional guidance on clinical trial delegation of authority logs.
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.