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...
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...
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...
Introducing CRIO Publisher, our highly anticipated new release! What’s good? CRIO eSource allows sites to build and save research-specific templates; capture data in real-time with protocol-specific edit checks; originate and respond to data queries; display automated audit trails; and share data with CRA’s without privacy concerns. What’s great CRIO Publisher allows eSource site networks, running the...
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,...
Leadership’s role in empowering emotional resilience and adaptation in the clinical research industry. For the last 25 years, the founders of BioNTech have been dedicated to using mRNA technology in the treatment of cancer. In January 2020, the company’s leadership identified that their innovative technology could be applied to a COVID-19 vaccine – and the...
Should we be learning how to cope with the complexity of remote/virtual monitoring, or is it more important that we learn to cope with change itself? How can industry stakeholders encourage and drive transformational change, while being mindful of the common thread that regulatory compliance must play in the framework? In Part 4 – QA/QC...
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...
Patient recruitment has long been a primary challenge within clinical trials. Looking to give your site an edge in 2021? In Part 2 of our dynamic 7-part webinar series, How Research Sites Can Win with De-centralized Trials, our panel of industry experts dives into patient recruitment. Topics covered over the course of 7 sessions include:...
For every clinical trial, the sponsor and/or a CRO will conduct a site selection process to determine what research sites are suitable to conduct their trial. A site’s ‘suitability’ is measured by a multitude of factors including but not limited to previous experience conducting clinical trials, research experience for a specific indication, resources available at...
In the latest virtual conference hosted by ACRP, Innovation in the Era of COVID, Raymond Nomizu of Clinical Research IO and Jessica Branning of ClinCloud Clinical Research discussed electronic Source (eSource) and how it has shaped the future of clinical research. Ms. Branning’s site, ClinCloud, was built ground-up on a technological platform centered around CRIO....
The last twelve months have been a year of unprecedented and transformative adaptation in clinical research. In this 7-part webinar series, industry experts share their collective reflection on decentralized trial modalities and their role in advancing the research of tomorrow. From e-Consent forms to remote patient monitoring, technology will continue to support this process. Sourcing...
