Check out CRIO’s recorded webinars, podcasts, and videos
Watch this on-demand webinar for a discussion of recent trends in clinical trial site network consolidation. The latest eBook, “The Rise of the Clinical Trial Site Mega Network” is the third installment in the “Scaling and Innovating” series by CRIO. In the first book in this series (published in 2019), CRIO predicted that clinical research...
Dr. Elena Christofides joins the SCDM podcast to talk with Linda King about the challenges and opportunities of using eSource from a site perspective. Dr. Christofides is an experienced global lead Principal Investigator with Endocrinology Associates, Inc. She has using eSource for more than a decade and shares some of the top challenges she has...
Abstract: Staying current with regulatory changes is important when it comes to staying out of trouble with regulatory agencies, maintaining your reputation, and successfully conducting clinical trials. Join Marc Wartenberger, Director Corporate QA & Compliance at CRIO, for a review of new regulations, guidance, and decisions from 2023 that will impact clinical research. Highlights include:...
Discover a groundbreaking webinar delving into regulatory innovations in clinical trials, assessing new tech compliance and enhancing data quality while reducing site and patient burdens. Innovation in clinical trials historically has been slow, and people often point to regulations and regulators as the reason. Are regulators truly the bottleneck? In this webinar, Jonathan Andrus makes...
Are you interested in investing in clinical trial software at your research site, but worried how your staff will adapt to the change? At Team CRIO, we partner with many sites who experience this challenge; that’s why we ensure you’ll have a dedicated project manager for your team. In this webinar, Luke Snedaker, the VP...
Find out how CRIO Reviewer, an integrated eSource/EDC platform, can help you reduce costs, improve quality, and eliminate costly enrollment delays on your next clinical trial. Our solution eliminates SDV, reduces on-site monitoring time, and increases enrollment rates by eliminating double entry into eSource and EDC systems. Schedule a demo to explore CRIO.
Never miss another re-consent with CRIO eConsent. Our solutions is fully integrated with our protocol driven eSource driving protocol compliance. Schedule a demo to explore CRIO.
Podcast date: July 25, 2023 Topic: Consented Patient Medical Records Automatically Populating In Your Clinical Research Source? In this episode of The Clinical Trials Guru with Dan Sfera, Dr. Joy Bhosai, CEO at Pluto Health and Raymond Nomizu, CEO at CRIO discuss the impact of CRIO’s Medical Records API. CRIO, in partnership with Pluto Health,...
CRIO’s eSource and EDC solutions drive protocol compliance, eliminate transcription, and save sites and sponsors time and money. Schedule a demo to explore CRIO.
Webinar Date: December 6, 2019 Webinar Guest: Sean Rice Track your clinical trial performance metrics to take control of your pipeline. Investing in the long haul means having robust business development capabilities now. That starts with data. Join Sean Rice, CEO of Medical Research Alliance and Co-Founder of Devana Solutions as he discusses the 5 metrics every...
Webinar Guests: Raymond Nomizu, JD, CEO of CRIO Lewis Edwards, Systems & Operations Lead at Linear Clinical Research Ltd. Linear Clinical Research is a research site located near ground zero of the first Australian death from coronavirus and is running life-saving cancer trials amidst an environment of significant travel restrictions. In addition to discussing how...
Clinical research is seeing widespread disruption as sponsors continue to pause their studies in light of the COVID-19 crisis. One industry expert, however, has observed a level of resilience in the responses from sponsors and research sites and predicts research will pick up quickly after the crisis is over. Rachel Truxall, corporate director of business development at...
