EHR’s aren’t built to support clinical research the same way as eSource This may be surprising to many, but it’s important to understand that an EHR is not designed to support the needs of a clinical trial. The EHR’s primary purpose is to give healthcare providers a flexible tool to document patient encounters and generate...
CRIO recently attended the Save Our Sites conference from March 13th to 15th in Oklahoma City, OK. It was an inspiring and energizing weekend that brought together research sites from around the world to share insights and challenges. Throughout the event, discussions spanned a wide range of critical topics, including site growth, financial sustainability, expansion...
With the emergence of new technologies and tools in clinical research, the burden on sites to keep up with the flood of new applications and software is especially daunting when it comes to user access and account management. As we’ve discussed in our previous blog post, Single-Sign-On (SSO) can help alleviate some of the burden...
With the increase in the use of digital platforms, managing multiple passwords across various applications and systems can quickly become a daunting task. As organizations expand and their digital footprints grow, the need for efficient and secure program access management becomes increasingly important. Because of this, many companies have implemented a Single Sign-On (SSO) system....
The Journal of the Society for Clinical Data Management (JSCDM) recently published the original research article “Comparison of electronic health records and electronic source data in clinical research trials: a retrospective review” which was co-authored by Amelia Tian, CRIO Solutions Consultant, and Olivia Dennis, CRIO Analytics and Data Migration Manager, alongside Dr. Elena Christofides (Endocrinology...
COVID-19 has fundamentally changed how clinical trials are conducted. In May 2021, FDA developed the ‘Resiliency Roadmap for FDA Inspectional Oversight’. In this document, FDA identified and embraced technological advancements by incorporating remote regulatory assessments (RRAs) into its inspection repertoire. During the pandemic, at a time where travel was restricted and personal contact heavily discouraged,...
Congratulations to CRIO President and COO Jonathan Andrus on the publication of “Best Practice Recommendations for Electronic Clinical Outcome Assessment Data Changes” in the Journal of the Society of Clinical Data Management. This long awaited publication, a joint effort by industry thought leaders in the area of clinical data, summarizes the guidelines for eCOA data changes developed...
Check out this article from TrialSite News about our newest eBook. The article, titled The Rise of ‘Mega’ Site Networks in For-Profit Clinical Research, highlights some of the key talking points from the eBook and includes insights from some of the team over at TrialSite.
Clinical research sites now get reimbursed for CRIO nearly half the time, at $2,000 per study Many clients ask if sponsors will reimburse them for the use of CRIO on their studies. Not long ago the answer was that sponsors sometimes did, but often it was an uphill battle. Now, sponsor reimbursement is becoming commonplace...
