CRA Solutions, Inc. is a full-service CRO with experience in the Medical Device, Drug/Biologic, Oncology, Interventional Cardiology, Organ Transplant, and Neurology fields. We offer complete clinical trial program management from the planning stage to FDA approval. We have partnered with leading companies, Universities (Investigator Initiated), and start-ups alike throughout all phases of product development.
The company was founded in 2000 by Jill Matzat (RN, BSN), a certified CRA and credentialed Clinical Research Trainer. We are a female-owned and owner-managed organization with the experience and expertise to manage all types of clinical research studies. CRA Solutions provides personalized attention and communication to meet our customers' needs. We offer focus, flexibility, and rapid response times.
At CRA Solutions, we understand the needs and goals of clients, and we are committed to delivering service excellence and high-quality results - on time, every time.
To excel at managing and monitoring clinical trials with a primary focus on professionalism, innovation, ethics, and quality.
Along with our sister company, Medical Research Management, we are committed to providing excellence in all aspects of clinical research management, monitoring and training.
Most problems during a clinical trial are caused by a lack of training and preparation, so we strive to prevent potential errors before they occur. We understand the importance of documentation, accountability, and oversight. Our monitors are trained to rapidly identify and remediate compliance issues using effective Corrective Action Preventative Action (CAPA) plans.
Our monitors are graduates of the MRM 140 Hour CRA Certificate Program or Advanced Quality Monitoring program. We believe that monitoring is a function of auditing, so our CRAs use the MRM Step Monitoring Method, study specific tools for accountability, to standardize the monitoring process and secure compliance.