Evolution Clinical Trials' mission is to provide high-quality and personalized research for our sponsors as well as to improve the health care of our patients through research.​ We are a group of responsible, caring, and trustworthy individuals committed to conducting phase I-IV clinical trials in the utmost professional, safe, and effective way. Always focused on maintaining a close relationship with our patients, sponsors, IRBs, CROs, and other vendors to ensure on-time completion of every clinical trial while promoting an atmosphere of harmony, team spirit, and career advancement. Our team possesses ample clinical trial experience, and it is directed on preserving respect towards subjects and protocol. This respect is accomplished through rigorous ethical codes and regulatory compliance, including adherence to Good Clinical Practice ICH - GCP, HIPPA, and FDA regulations. We offer experienced, trained, and bilingual personnel (English and Spanish) who interact with our subjects, sponsors, and CROs as a cohesive team. Turnaround time for Regulatory Documents, budgets, and contracts is usually 24 to 48 hours.