Biopoint
Boost patient safety and elevate the quality of care with BioPoint, a comprehensive software suite tailored for Veterans Administration and surgical facilities.
Boost patient safety and elevate the quality of care with BioPoint, a comprehensive software suite tailored for Veterans Administration and surgical facilities.
Designed for site efficiency, Advarra’s eSource + EDC supports seamless data capture and remote workflows, minimizing duplicative efforts.
Achieving diversity, equity, and inclusion (DEI) in clinical trials is crucial for producing comprehensive and effective medical research benefitting all
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Onsemble Conference 2025 The Premier Technology Conference for the Clinical Research Site Community Join your Site and Institution peers to
This white paper examines four KPIs most impacting timelines and budgets and offers strategies for effective communication and risk mitigation.
Clinical research is complex and resource-intensive, and to understand just how far an organization’s resources can go, assessing a study’s
A regulatory binder is essential for managing clinical trial documents, ensuring regulatory compliance, and facilitating audits. It organizes critical documents;
The only constant in clinical research is change. Researchers are always innovating, making it a necessity to navigate complex organizational
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Every site is different. Learn how to meet their unique needs and make workflows and collaboration more efficient in this blog.
Every day, clinical research organizations work to deliver a seamless user experience for their staff, while also providing robust security