BMA was founded in 1993 by Barbara McLaughlin, R.N., who had firsthand experience with the challenges of study start-up, maintenance, and closeout. Timely receipt and submission of all FDA required documentation throughout the life cycle of clinical trials was the driving force behind the creation of BMA.
Over the past 18 years, the company has advanced into many areas
of clinical trials support requiring quick, efficient turnaround
of clinical and regulatory documentation and data throughout
the world. Our success has resulted from an unchanged approach
that has stood the test of time – provide quality, commitment,
excellence and value to our clients in order to support their
clinical trial needs.
BMA remains a specialized CRO, employing clinical and regulatory professionals with experience in the pharmaceutical, device and medical industries with backgrounds in Study Management, Data Management, Nursing, and Clinical Research Monitoring. Understanding your need to stay within budget, we provide our expertise at a highly competitive rate. We believe that quality should never be sacrificed to keep costs in line.
At BMA, we strive to develop a true partnership with our clients. This has proven to be the most mutually beneficial approach, providing excellent results for both the study team and project. At BMA, we make every effort to work with you, not simply for you. We welcome the opportunity to familiarize ourselves with your processes and unite them with our own, creating a cohesive, dynamic work team. Our highly customizable team and services can be modified quickly to help you achieve your goals.
Our commitment to our clients and their projects, as well as the consistent quality of our work is the foundation of our company. Tell us your needs and we will work to provide a comprehensive solution for you.