Industry knowledge, webinars and more for clinical research sites
It’s easy to get started with CRIO’s Medical Records API with these 6 steps. This blog post will help you set up and be ready to go in just over an hour. If you haven’t already signed up for the Medical Records API, click here for more information, reach out to your customer success representative,...
DALLAS, Aug. 14, 2023 – The Association of Diversity in Clinical Trials (AOD) and CRIO, a leading eSource technology provider, are excited to announce a new partnership. CRIO’s software platform empowers research sites to run more effectively, enabling research in underserved communities. CRIO’s work aligns with AOD’s mission to establish standards and best practices for the...
What is eSource? According to the FDA, eSource is defined as “data initially recorded in electronic format. They can include information in original records and certified copies of original records of clinical findings, observations, or other activities captured prior to or during a clinical investigation used for reconstructing and evaluating the investigation.” eSource is already...
In clinical trials, patient safety is paramount. Once a subject is randomized into a clinical trial, they undergo a series of treatment procedures. Any changes in their medical status, including alterations in medication or occurrence of Adverse Events (“AEs”), need to be recorded. These changes are typically noted by site staff in a document known...
In our previous blog post, “Navigating Medical Records Acquisition in Clinical Trials,” we unpacked our solution for the time consuming process of sourcing patient medical records. In this followup, we’re addressing the challenge of inaccurate and incomplete EHRs in clinical research. Electronic Health Records (EHRs) form the backbone of healthcare data. However, when it comes...
Navigating medical records acquisition in clinical trials is a time consuming challenge faced by clinical research sites. Electronic Health Record (EHR) systems play an integral part in this process, serving as critical repositories of patient data. Yet, the lengthy process required to access these records often complicates the patient screening process. Subsequently, this impacts enrollment...
In this blog post, Hannah Kulkarni, Customer Success Manager II at CRIO, caught up with Dr. Lovie Negrin, founder and director of research at Randomize Now, for an insightful conversation. Together, they dissect the impact of how Dr. Lovie’s efforts are increasing diversity-driven clinical trials. Who is Dr. Lovie? Dr. Lovie Negrin is the founder...
Innovative solution benefits patients with access to clinical trials as a treatment option, ongoing personalized health insights, and ultimately speeding new treatments to market BOSTON, MA, July 19, 2023 – CRIO, a Boston-based healthcare technology company, in partnership with Pluto Health, a Durham, NC-based smart care coordination service company, announces the development of a scalable...
EMR Integration: The Challenge In the past several decades, Electronic Medical Record (EMR) systems have become the standard in documenting clinical care in the United States and many other countries, while Electronic Data Capture (EDC) systems have become standard in global pharmaceutical trials. Naturally, the industry has been highly focused on the tantalizing possibility of...
In order to increase diversity in clinical trials, it is important to include voices from many different communities and roles. For this blog post, CRIO employee Stefanie Palmer sat down for a discussion with Dr. Hadi Danawi to talk about involving the Arab American community and people from Middle Eastern backgrounds in clinical research. Who...
Thousands of sites around the world have embraced site-facing tools such as eSource, eISF, and eConsent. These technologies are now a routine part of the clinical trials landscape. Yet, we still often hear sites expressing their belief that they need sponsor approval to adopt their preferred electronic source platforms, like CRIO eSource. That is simply...
Over 70% of clinical trial data today comes from non-case report form data. Non-case report form data includes continuous data such as wearable data, lab data, patient reported data and ECG data, to name a few. Generally speaking, these are all collected as source without transcription or entry into another system. Today, we have reached...
