Let’s face it, we have a paper problem. In a recent webinar, RealTime’s CEO, Rick Greenfield spoke about the existing “paper problem” in the clinical research industry and ways that we can overcome it to achieve “Paperless Nirvana”. As you already know, the Clinical Research Process primarily functions off of paper source documentation and manually … Read more
You’ve adopted RealTime-PAY because your subjects and their experience are your main priority. Our system has helped your site reimburse patients for their time and travel with innovative technologies such as direct deposit and an online portal. Consequently, YOU are our main priority. Our team of experts works night and day to provide you with … Read more
A few years ago, eRegulatory systems were nothing more than sponsor-fed trial master files requiring sites to complete double, and sometimes triple, the amount of work. Anytime site regulatory personnel heard “electronic regulatory” they cringed at the idea of interrupting their day-to-day flow to maintain these systems in addition to their paper binders. Due to … Read more
You have probably heard the term S.O.M.S., but what does it mean? Quite simply, SOMS stands for Site Operations Management System. It rhymes with Tom’s… it’s SOMS! OK, now you can say it, but what is it? In the vast arena of software available for clinical research sites, there is a lot to navigate and … Read more
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
Did you catch our webinar hosted by ClinEdge, “e-Regulatory Systems – Connecting Sites and Sponsors in a Whole New Way” from August? If not you can watch the recording here. Nathan Levens answered several great questions during the webinar and received additional questions after the webinar ended. Below are some additional questions addressed after the webinar. … Read more
With Part 11 compliant systems now available for investigator sites to streamline processes, some of us are wondering what exactly is 21 CFR Part 11 and why is it important? Essentially, 21 CFR Part 11 regulations define the criteria under which electronic records and electronic signatures are considered trustworthy, reliable, and equivalent to paper records. … Read more
When sponsors and CRO’s talk about good sites, there is a huge amount of emphasis placed on one critical factor; the ability of a site to meet recruitment goals. One misconception that sponsors and CRO’s seem to have is that research subjects come out of a doctor’s own practice. There are always exceptions, and certainly … Read more
What Makes a Good Site CTMS? [by: Rick Greenfield] In the course of searching for a good CTMS solution, many site stakeholders are faced with the challenge of determining which of the CTMS products currently on the market are going to be the right fit for their site and personnel. What makes evaluating and selecting … Read more
Site Recruitment Tactics – Linking with CTMS [by: Rick Greenfield] There are many clinical research sites that have discovered the benefits of web-based advertising for study-specific recruitment, general site branding and database building. Most sites are not linked up with a CTMS to track the effectiveness of individual advertising runs and manage outcomes of every … Read more
