Encouraging Site Centricity and Collaboration at Onsemble
During the week of October 5-8, more than 1,700 Advarra technology customers gathered virtually for the Fall Onsemble Conference. A
During the week of October 5-8, more than 1,700 Advarra technology customers gathered virtually for the Fall Onsemble Conference. A
More often than not, researchers face screen failures during the study activation process. Screen failures occur when research staff put
Academic research institutions may not face the financial scrutiny of commercial sites, but they still need proper funding to support diverse initiatives.
While electronic source data collection is not new, collecting source data in a variety of settings in a compliant manner is. With this in mind, how does one maintain data quality and integrity while ensuring participant safety and staying compliant?
Informed consent, a cornerstone of ethical research, involves describing important elements of research in a way that permits participants or
The landscape of data privacy is certainly dynamic and, at times, imposing. In particular, transferring data across borders can be difficult to navigate.
At Advarra, it’s our mission to ensure safer, smarter, faster clinical research every step of the way in the research
Here are four questions to ask during the CTMS selection process to offer more insight into your future success with the selected vendor.
Phase I research demands careful IRB oversight, balancing participant safety with timely reviews. Proactive strategies can help address its unique challenges.
This blog covers three must-have decentralized trial tools to efficiently and compliantly implement remote modalities at your organization.
eSource, ePRO, and EDC each play distinct roles in clinical trials, enhancing data consistency, participant experience, and overall study efficiency through technology integration.
Research organizations utilize a variety of medical professionals to conduct successful clinical trials. Two of those positions are a medical