Medrix Clinical Research was established in the year 2019 by a group of professionals from the clinical research, pharmaceutical and health care industry with rich and varied experience.
In usual practice, site management activities depend on the clinical research associate's capabilities. However, in complex studies, Medrix Clinical Research has extended its site management Services through a Site Management Organization. Medrix Clinical Research collaborates with medical institutions (Hospitals, Medical Colleges and/or Clinical Research Institutions) in North India to enhance the site's performance at the site level. The benefit of this practice is that it ensures robust patient recruitment and retention. We focus on quality and add value to our client’s clinical development programs by evolving various strategies to ensure timely execution of clinical projects within the budget.
Medrix Clinical Research works with clients across globe to conduct the Phase II to Phase IV clinical trials involving pharmaceutical, biological and medical devices products. Our expert team of investigators, Project managers and study coordinators are committed to provide high quality data and ethical standard within the time frames. Medrix Clinical Research provides the complete site managements solutions for the Site, Sponsors and CROs Pre-Study Site Selection to close out. We provide the Record Management and destruction Services.
