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decentralized trials

Running a Site 3 Minute Read

Never miss another re-consent: The benefits of an integrated eConsent-eSource solution

With the recent push toward Decentralized Clinical Trials (DCTs), many sponsors are adopting eConsent. eConsent allows patients to consent electronically, whether in clinic or remotely, from the convenience of their home. eConsent offers sponsors, CROs, investigators and patients these benefits: Reduce errors by ensuring completion of all fields Automated audit trails ensure accuracy of date-times...

Running a Study
2 Minute Read -

Ask Me Anything – Hitting the Target with Good Study Design

Mary Brenner, MSN MArch RN, is CRIO’s Study Design Manager and brings deep-rooted expertise as a registered nurse to CRIO’s in-house study design team. In this quick Q&A, Mary shares the benefits of good study design for sponsors and sites, the downstream effects of standardized study designs, and gives tips for designing it on your...

CRIO Company News
2 Minute Read -

CRIO announces the launch of another industry first. Introducing, CRIO Reviewer EDC (eSource/EDC)

CRIO, the leader in eSource technology, is announcing the launch of an industry first, CRIO Reviewer EDC, designed to create a fully integrated eSource/EDC system. Reviewer EDC allows sponsors and CROs to review, query, extract, code and lock data collected in the CRIO eSource application within minutes of site completion. This solution enables research sites...

Running a Study
2 Minute Read -

eSource unlocks true remote monitoring benefits

Mark Joing is the Founder & CEO at Mojo Trials, a startup life sciences service provider delivering virtual site monitoring in clinical trials. He is also the Chief Operating and Financial Officer at Sanaby Health, a Special Purpose Acquisition Company created to accelerate innovation in healthcare. His 25+ year career in biopharma includes executive roles...

eSource makes the eCRF reliable
Running a Study
2 Minute Read -

eSource makes the eCRF reliable, accurate and timely

Bridging the gap eSource is the bridge between the protocol and the eCRF fields. To understand why, we need to understand what each does. The protocol describes the purpose of the study, the core hypotheses, the endpoints that are to be collected, and the resulting procedures to be performed to support those endpoints. The eCRF...

CRIO Company News
1 Minute Read -

CRIO Continues Record Growth for 2021 as Customers Recognize Value and Efficiency Gains of eSource

CRIO, a Boston-based technology firm streamlining clinical trials for sponsors, sites and patients, announced a fifth consecutive year of record contract bookings and revenue for 2021. Highlights for CRIO’s breakthrough 2021 include: Record YTD contract bookings and revenue – bookings up 80% year over year Over 300 new sites, including 5 of the top 10...

Running a Site
2 Minute Read -

Key Takeaways from the 2021 SCRS Site Solutions Summit

Reflections on the Summit The 2021 Global Site Solutions Summit, hosted by the Society for Clinical Research Sites, was an amazing event. The first in-person event that our company has attended in 18 months, the Summit provided an opportunity for CRIO to meet new people and reconnect with clients and friends alike. Post-Pandemic Trends, Here...

3 Reasons Principal Investigators Need eSource
Running a Site
3 Minute Read -

Building Better Oversight – 3 Reasons Principal Investigators Need eSource

What’s wrong with the way that most sites have been recording data for decades? While much of research data is still being collected on paper, digital adoption across source, regulatory and remote monitoring is rapidly increasing among sponsors, CROs, and research sites. Many of the challenges that Principal Investigators (PIs) face during the conduct of...

decentralized clinical trials
Running a Site
1 Minute Read -

Clinical Research IO’s latest survey shows that clinical research sites have adopted widespread technology in response to the rise of decentralized clinical trials

Clinical Research IO (CRIO)’s recent site survey showed that most sites have recovered business lost during the pandemic, are adjusting to the decentralized clinical trial model, and have implemented their own software in response. At the beginning of the pandemic, CRIO conducted a survey to look at the impact of coronavirus on research sites. By...

CRIO
Running a Site
2 Minute Read -

3 Reasons You Should Be Using CRIO’s Custom Reports

Standard versus Custom Reports Every site has its own definition of success. As a clinical research site owner, manager, or medical director, you might be considering a deep dive into your analytics to guide decision-making and demonstrate progress to stakeholders. Sometimes, Standard Reports can get you just what you need. Standard Reports are report templates,...

Remote Consenting
Running a Site
1 Minute Read -

How Research Sites Can Win with Decentralized Trials – Part 3 – Remote Consenting

Remote consent is one of the main technological and operational advantages that support direct-to-patient recruitment. In Part 3 of our 7-part webinar, join the conversation around the willingness to adopt remote consenting services, as well as the challenges of multinational clinical trials covering different languages. Topics covered over the course of 7 sessions include: Part...