Sites have a million things to deal with before, during and after a trial. Coordinators and staff have their plates full every day with paperwork, meetings and hundreds of emails. Starting a new study is not easy, but it can be a whole lot less stressful with the right CTMS. Choosing the perfect CTMS will … Read more
Barry Lake, CEO, Devana Solutions, LLC (CHARLESTON, SC) November 30th, 2017 — An ongoing industry consolidation of contract research organizations (CROs) whose services are used by large drug manufacturers is a significant trend that will only increase in the days to come, says Barry Lake, chief executive officer at Devana Solutions, LLC. Sponsors are putting … Read more
The holidays are upon us. As Thanksgiving and Christmas approach, you’ll most likely see your patient retention rates drop. While we are all looking forward to the Holidays and spending time with loved ones, subject no-shows can have a negative effect on your trial and your site’s bank account. So, how can you motivate your … Read more
The clinical research industry has inevitably been slow to adopt technological advances primarily due to regulatory constraints and a fear of change that could disrupt current processes. While the regulatory guidance has been issued by the FDA, development of solutions that can conform to the guidance AND improve efficiency is challenging. In the recent years, … Read more
(CHARLESTON, SC) Oct. 19, 2017 /PRNewswire/ — Site selection for clinical trials is one of the biggest headaches for pharmaceutical Sponsors and CROs, with almost half of sites enrolling zero or one patient. Those under-performing sites annually cost Sponsors over $4 billion globally excluding opportunity costs. Today, Devana Solutions® announced the release of MATCH PERFORMANCE, a powerful new cloud-based system to provide … Read more
As a clinical researcher, being at your desk to take care of study documentation, patient referrals and everything else that goes into managing your studies can be difficult and time-consuming. That’s why our team has created a mobile app that lets you access all your files, contacts, patient referrals, and inclusion/exclusion criteria on the go. … Read more
Research sites can now access popular eDOCS solution on mobile device with new app SAN ANTONIO—Want to access site eRegulatory files, sign documents with your thumb print, refer a patient to a study or look up site and sponsor contacts all on your mobile device? There’s an app for that! RealTime-CTMS launched the first-of-its-kind new … Read more
How many checks do you sign each day? Ten, twenty, fifty? You issue a check to your subjects after every visit but, how well do you know the person who will cash the check? Can you trust them with your information? Every issued check represents a higher risk of fraud for your company. It will … Read more
As a RealTime-CTMS user, you are likely accustomed to the quick access that RealTime gives you to study and subject information. Our CTMS allows you to easily manage your subject data, study information, study visits, scheduling, financial data, reports, and more. But did you know RealTime also has a TEXT feature that fully integrates with … Read more
Let’s face it, change is hard. You get used to the way you’ve always done things and when someone talks about doing something different, you’re like a deer caught in headlights. If you’re working at a clinical research site and have always used paper regulatory documents, changing to an electronic document solution may seem overwhelming … Read more
RealTime eClinical Solutions is a leading, enterprise-grade technology provider facilitating global clinical trials with a comprehensive eClinical platform. Purpose-built for clinical research sites, site networks, academic medical centers, sponsors, and CROs, the platform goes beyond traditional CTMS to empower research and business workflows for modern-day clinical trials.
