3 Essential Elements of Change Management Within Clinical Research Operations At Your Research Site
The key to effective, productive change within a research institution lies at the nexus of people, process, and technology.
The key to effective, productive change within a research institution lies at the nexus of people, process, and technology.
Gathering high-quality, reliable and statistically sound data is the goal for every clinical trial; and effective data management is essential to ensuring accurate data collection, entry, reports and validation. As a critical phase of the clinical research process, it’s important to establish and maintain organization-wide standards for data management to ensure consistency across all individuals and teams involved.
Subject safety and reliability of data are paramount in clinical research. This blog outlines what auditors look for when performing source data verification (SDV) and source data review (SDR) during routine investigator site audits.
Advarra is excited to introduce Fireside Chats, a series of virtual conversations discussing current issues in clinical trials. Each Fireside Chat brings together perspectives from across the research community, enabling real-time discussion of contemporary challenges and potential solutions to help make research altogether better.
On Clinical Trials Day, now more than ever, it’s important to recognize and thank those unsung heroes at the focal point of research: research sites and institutions.
As we near the end of 2019, let’s take a look back at the blogs that generated the most interest this year from readers like you.
On September 5, 2019, Advarra announced its intent to acquire Forte. The combined organization leverages mutual strengths in supporting the research community with client service, regulatory expertise, and technology-enabled efficiencies to accelerate innovation, streamline research operations, support faster study start-up, and help make research altogether better. Click here to read the full press release.
On March 5, 2019, Advarra announced its acquisition of Quorum Review IRB and Kinetiq, the research and technology consulting division of Quorum. We’ve assembled this FAQ to address some of the most commonly asked questions about the acquisition and integration.
The Advarra team is proud to announce that all major integration activities are now complete. SOPs have been harmonized; staff
The Advarra team has worked to fully integrate our processes and policies to provide clients with unified capabilities and support
The Advarra team (formerly Chesapeake IRB and Schulman IRB) continues to integrate our processes and policies, leveraging mutual strengths in
Since November 2017, the Advarra team (formerly Chesapeake IRB and Schulman IRB) has been working to integrate our processes and