RAB Services Page

Advancing the Next Generation of Clinical Investigations.

About RAB

Who We Are

We are a Site Management Organization specializing in the management of clinical investigative sites located throughout India. Research Across Borders focuses on providing superior service to the pharmaceutical, biotechnology and medical device industries through the outcome of successful clinical trials.

What We Do

We provide qualified, pre-screened, principal investigators to our Sponsors and Contract Research Organizations for participation in clinical trials. We also provide invaluable resources and services to our participating physicians. All of the Investigators within the Research Across Borders network have been evaluated to ensure they are not only qualified to conduct clinical trials, but have the patient population and administrative capabilities to properly conduct them. By placing studies through our company sponsors eliminate a significant amount of time and expense when attempting to qualify, enroll, and initiate a site.

Our Sites

All of our sites have access to our exclusive education and training programs which consist of: ICH/GCP training, working with Institutional Review Boards, subject consent process and regulatory document retention and archiving practices, just to name a few. We are committed to continuously educating and training our physicians and site personnel, which assures us that all of our sites conduct clinical trials to the highest possible standards in existence. The sites in our network are carefully selected based on their training, education and clinical study experience. We also select sites based on their ongoing commitment to adhere to the strictest of regulatory standards, which assures our sponsors an uncompromised level of quality data obtained through our sites. All of our physicians also have access to our quality assurance resources which aid in maintaining regulatory compliance.

Study Subjects

We vigilantly assess the subject populations at each site from which study subjects will be drawn to assure the increased likelihood of enrollment goals being met. When necessary we work with each individual site to assess various advertising media to assist in meeting recruitment objectives. Our goal is to meet if not exceed our Sponsors recruitment timeline metrics!

Site Communication

The cornerstone of any successful clinical investigation is ongoing support and communication between all parties. Because of our commitment to the successful outcome of every study in which we participate, an internal site manager is assigned to each study to ensure that communication is maintained and that the study receives the full attention it deserves until completion. We maintain ongoing communication with each of our sponsors and sites to identify potential issues before they can become a problem. It is our philosophy that communication is the backbone to successful working relationships.