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
sites
Screen Failure in Clinical Trials: Improving Reconciliation
More often than not, researchers face screen failures during the study activation process. Screen failures occur when research staff put
Leveraging Data to Lead and Manage the Research Mission
Academic research institutions may not face the financial scrutiny of commercial sites, but they still need proper funding to support diverse initiatives.
Beginner’s Guide to Compliant Electronic Source Data Capture
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?
Research Equity and Enrolling Non-English Speakers
Informed consent, a cornerstone of ethical research, involves describing important elements of research in a way that permits participants or
Understanding International Data Transfer’s Impact
The landscape of data privacy is certainly dynamic and, at times, imposing. In particular, transferring data across borders can be difficult to navigate.
Ensuring a Successful and Collaborative SDLC Process
At Advarra, it’s our mission to ensure safer, smarter, faster clinical research every step of the way in the research
4 Questions to Ask CTMS Vendors
Here are four questions to ask during the CTMS selection process to offer more insight into your future success with the selected vendor.
IRB Review of Phase I Research: Balancing Ethics and Efficiency
Phase I research demands careful IRB oversight, balancing participant safety with timely reviews. Proactive strategies can help address its unique challenges.
3 Must-Haves to Deploy Remote Clinical Trials
This blog covers three must-have decentralized trial tools to efficiently and compliantly implement remote modalities at your organization.
Understanding eSource, ePRO, and EDC
eSource, ePRO, and EDC each play distinct roles in clinical trials, enhancing data consistency, participant experience, and overall study efficiency through technology integration.
Understanding Medical Science Liaisons and Clinical Liaisons
Research organizations utilize a variety of medical professionals to conduct successful clinical trials. Two of those positions are a medical