Founded in 1997, RCTS has grown steadily in both size and reputation over the years thanks to our commitment for delivering exceptional quality to our customers.
What began as a two-person enterprise operating in a 1,000 square foot leased space is, today, a fully equipped, state-of-the-art, 16,500 square foot testing center that employs a team of more than 30 talented Clinical Research Coordinators (CRC), Clinical Research Technicians (CRT), QA personnel and recruiters who are committed to the highest standards of clinical testing.
Our approach to clinical testing is based on the following tenets:
Understanding the Sponsor's Goals
Understanding the sponsor's goals is paramount to ensuring a successful clinical trial. RCTS works closely with each sponsor to ensure that goals, roles, and responsibilities are clearly defined. On-site investigator meetings, coupled with protocol development and review, help ensure a successful clinical trial.
Assembling the Clinical Team
RCTS approaches all clinical trials with the understanding that assembling the right team of medical investigators, sub-investigators, clinical coordinators, quality assurance personnel, and clinical technicians is critical for the success of the trial. Our medical investigators are all board-certified in their specialties, and all clinical staff members are trained in cGCPs. Additionally, our clinical recruiters work closely with the clinical trial team to ensure subject recruitment adheres to the inclusion/exclusion criteria outlined in the protocol.
Working with Sponsors throughout the Clinical Trial Process
Our clinical team works closely with each sponsor throughout the clinical process to ensure that timelines and clinical goals are being met. From protocol development through submission of the final report, frequent communication with the Sponsor is maintained. Additionally, many sponsors use RCTS in a turnkey fashion, entrusting all aspects of the clinical trial process to us. RCTS is capable of providing the following to all of our sponsors:
- Protocol Development
- Submission of All Necessary Clinical Documents to an IRB
- Case Report Form Development
- Statistical Analyses of the Clinical Data
- Final Report Prepared According to ICH-GCP Guidelines
At RCTS we are committed to providing unparalleled service and quality to ensure the successful execution of our sponsors’ clinical trials.
It’s our commitment to both quality and service that has attracted some of the world’s leading consumer product and pharmaceutical companies—as well as quality-conscious start-ups—to our list of satisfied clients.
In addition to providing the best in technical execution of clinical trials, RCTS is known for providing on-time updates and final reports.