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 is a leading and visionary clinical research organization in Canada and the US.

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.

Not only are new drugs being developed, but existing compounds are also being continually altered and tested to address additional therapeutic conditions. Over 15,000 clinical trials take place worldwide each year and that number will continue to increase as regulatory bodies such as the FDA, Health Canada, and the European Medicines Agency require increasingly more clinical trials to be conducted per new drug application.

Clinical trials can provide extremely effective treatment options for patients. Physicians and nurses involved in clinical trials provide precise care and closely monitor the health of each individual enrolled in a trial and record protocol data which is confidentially collected by the trial Sponsor (Pharmaceutical company).

Patients who participate in clinical trials receive the latest treatment options which may prove to be more effective than treatments currently available on the market today, typically at no cost to the patient. Patients have the satisfaction of knowing that they are receiving exceptional care and also paving the way for future generations to come, who may benefit from that treatment when it’s approved for sale by health and regulation authorities.

Global Clinical Software Solutions

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.

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.