We work to provide the industry’s most rigorous standards in the conduction of clinical trials that allow pharmaceutical companies to determine the effectiveness, value and safety of drugs. It includes a research team with more than 10 years of research experience, and the human resources with medical background in United States of America and other countries. Our Research Facility has research professionals with the ability to conduct clinical trials in Phase II, Phase III and Phase IV.
Our medical network includes medical specialties such as Family Medicine, Pediatrics, Neurology, Cardiology, Ophthalmology, OB-GYN, Internal Medicine, Radiology, Dermatology, Podiatry, Pulmonology, Psychiatry, among others. The network and recruitment strategies have ensured the growth of our internal database with over 4500 patients for all medical conditions. By staying abreast of these changes and growing our portfolio of services to meet modern demands, we strive to remain valuable partners with pharmaceutical companies.
Enrique Pelayo MD
The Principal Investigator has the primary responsibility for ensuring the ethical conduct of the research study. This includes protecting human subjects’ rights, safety and welfare, protocol compliance, and adherence to institutional, state and federal regulations and guidance. The PI is responsible for ensuring informed consent is appropriately obtained from each participant and for appropriately maintaining study records. The PI is also responsible for complying with the financial and administrative policies and regulations associated with the award, overall fiscal management of the project, and conflict of interest disclosure.
Meet The Team