About Entralogix

Entralogix is the only fully integrated clinical research institute offering clinical, software, educational and consulting solutions. Entra comes from the latin word Entrata, which means the act of entering and a place by which to enter. Logix comes from the ancient greek word Logistikos, which is an operational word meaning the process of planning, implementing, and controlling the efficient, effective flow of services, related information and work from their point of origin to point of execution for the purpose of satisfying customer requirements. Our mission is to continue to satisfy our customer requirements by adding value to your clinical trial projects. Entralogix is uniquely positioned to add tremendous value at the level of the clinical trial site. Working along side physicians to conduct your clinical trials is our specialty. Our vision is simply. Our employees work directly with physicians at the point of execution to deliver the highest level of quality. Research For You, With You.

Clinical Research at Entralogix

Entralogix Clinical Research Institute has been conducting clinical trials in North America for Life Science companies since 2004. Clinical trials are a critical component of our health care system and are necessary in order to develop new drugs and therapies to improve our health.

Our consortium of research physicians practicing in community, universities, health systems and hospitals have participated in over 200 clinical trials and have enrolled over 4000 patients. We share a common clinical trials platform, as well as standardized processes, to achieve economies of scale. The consortium offers one-stop shopping for sponsors and the NIH with a single point of contact, one legal contract, one trial budget, one institutional review board (IRB), and one IT platform, yielding dramatic improvements in the speed, quality, and cost of trials.

Recruiting from deep within the local market's primary-care practices, patient accrual rates rise 2-3 fold. The integration of standard operating procedures (SOPs), processes, and technology ensures an optimized platform that delivers real-time, high-quality data to the study sponsors. Common SOPs allow physicians and nurses to focus on science, safety, and quality — not process. Entralogix has proven that any physician can integrate themselves in to a structured clinical trial platform, and with dedicated on-site research nurses, be a top performer on any clinical trial.

Our consortium works symbiotically with sponsors and CROs. Sponsors tend to want a customized and flexible approach, while still expecting the efficiencies of experience and technology. Entralogix aligns the needs of sites and sponsors. We are uniquely equipped to streamline the process in ways that Sponsors and CROs — with no direct access to patients — cannot.

Global Clinical Software Solutions

For years Pharmaceutical companies have used robust, secure and intelligent electronic systems to manage their clinical trial documents and Essential Trial Master File documents. Unfortunately, many of these gains in quality, time and cost savings were canceled out by paper based Site Investigator Binders/Files, otherwise known as the “last mile” problem. Giving external clinical partners such as Investigators, IRBs and Central Labs access to your Enterprise Document Management System and Trial Master/Site File system is not good I.T. practice.

eStudy Binder is the only comprehensive regulatory electronic Trial Master File fully integrated with electronic Investigator Site Files in a multilingual, enterprise secure system. Through seamless integration of all reguatory trial documentation, direct access to data and information, eStudy Binder reduces study start-up by 50%. Ongoing maintenance of Trial Master and Investigator Site Files is significantly reduced. Study close-out is reduced from weeks to hours.

Dramatically reduce administrative time for clinical studies with eStudy Binder's Rapid Study Start-up feature. Our 7 step process, combined with a comprehensive series of libraries and industry leading study cloning functions makes it possible to set up an entire study in less than 30 minutes.

Secure, IBM Enterprise Level, Electronic Clinical Trial Document System designed to manage the Investigator Site Regulatory Binder. Easy to use, intuitive binder design and powerful. Includes regulatory compliance checks, electronic documents, electronic workflows, tasks, electronic signatures.

If you are a Life Science company considering EDC for your next clinical trial, ask us about eStudyBinder^TM.