Whether you’re a pharmaceutical company, biotechnology firm, medical device company or naturaceutical company, EntraLogix can assist you with your clinical trials and testing requirements.

Pharmaceuticals face an ever-increasing requirement by regulatory bodies (such as the Food & Drug Agency, Health Canada and European Medicines Agency) to perform more and more tests and clinical trials per new drug application. At considerable cost, internal resources at these Pharmas constantly search for new physicians who are willing to absorb the workload and participate in clinical trials.

EntraLogix has a growing stable of qualified associate Investigator sites in a diverse range of therapeutic areas. All of our investigators are personable and have been carefully selected for their experience, large patient base, and eagerness to participate in clinical trials.

Supported by our EntraLogix team, which includes Project Managers, Regulatory & Ethics, Trial Administration, Registered Nurses, and call centre staff, our physicians have the ability to concentrate on administering exceptional patient care for trial participants.

With one phone call, your Pharma can select pre-approved Investigator sites in a matter of hours and receive a Project Manager to assist with all aspects of your trial. You’ll also receive an experienced GCP-trained Clinical Research Coordinator who will assist our physicians to achieve target enrolment quickly and provide exceptional patient care which ultimately increases subject retention and the success of your trial.

If you’re conducting an upcoming clinical trial and require assistance to achieve your patient enrolment requirements or wish to select pre-qualified physician sites, give us a call today and find out how we can assist your organization to achieve it’s clinical trial goals.