We are bringing innovation, quality and diversity to clinical research. We are a multi-functional team helping our partners conduct high quality trials with emphasis on patient-centered recruitment, expert site management, and regulatory affairs proficiency.
Patient and site enrollments is one of the biggest challenges in clinical development and drug trials. Working with our network of clinics and providers across the country, we research and expand access to research sites, and deliver more patient from fewer sites in less time. Our focus is on maximizing patient delivery, through innovative and predictive recruitment, providing customers with more patient per site, and reducing enrollment time overall, with resultant cost savings.
We are steadily and progressively increasing our site network capacity and partnerships. These relationships are part of our trifecta for accelerating patient enrollment and engagement while maintaining quality. We leverage our enduring relationships with independent physician associations to expand our strategic partnerships, to facilitate study setup, investigator training and study execution.
We provide innovative training and investigator meeting support to our strategic partners as well as the pharmaceutical industry. Our training solutions help to improve the efficiency and effectiveness of the study sites, regardless of the trial size, therapeutic area or study phase.
To build an environment of care and trust, and to empower physicians and patients, researchers and progressive pharmaceutical companies to work together to achieve a healthier future through medical breakthroughs. Our goal is to be the nexus that facilitates the development of leading edge treatments and pushes the boundaries of science by closing the gap between clinical research and clinical health care.
From pre-clinical to post marketing, we have excelled in achieving unconventional results from rapid site startup, successful completion of enrollment and the timely lock of the study database, to transforming clinical trial safety from a requirement to a key driver of program success
Bernard Mannes Baruch.
Clinical trials are integral part of clinical research and at the core of all medical futures. Clinical trials always find means to prevent and treat disease. The Trial may be new drugs or new combinations of drugs, new surgical devices or new way to use existing treatments. The ultimate purpose of clinical trials is to determine if a new test or treatment is safe, and if possible, actually works.
Volunteering for a clinical study is a personal choice. You have no obligation to do so, and participation is not right for everyone. After enrolling in a study, you may leave at any time for any reason.
Clinical studies questions
Phone: 240-237-7327
