At Spotlight Research Center, we prioritize the involvement of our Principal Investigators (PI) in every study. From feasibility assessments to staff training and obtaining informed consent, our PI’s are actively engaged. We place utmost importance on patient safety, ensuring that our staff stays up-to-date with Good Clinical Practice (GCP) training and holds relevant certifications. Our PI’s and Clinical Research Coordinators (CRC) diligently track and secure all study drugs. Data is meticulously entered into the Electronic Data Capture (EDC) system and cross-checked by our Senior CRC to maintain accuracy and integrity.

We strictly adhere to ICH, GCP, and regulatory guidelines, along with our own rigorous procedures. With our expertise in volunteer recruitment and screening, as well as our expansive network of experienced investigators, we conduct trials with subjects of all types. Our facility is designed to provide optimal efficiency, safety, and comfort, ensuring a positive experience for our participants.