Pioneering progress one trial at a time, shaping a healthier tomorrow together.
Cardio Health Clinical Trials is a research division of Cardio Health, with over 18 years of collaborative experience in working with multiple pharmaceutical companies on clinical trials from Phase II through Phase IV.
CHCT caters to multiple therapeutic areas with primary focus on Cardiology, Oncology and Gastroenterology with a versatile team of skilled cardiologist, oncologist, gastroenterologist and specialist in other medical fields.
CHCT specializes in addressing all matters related to quality, safety, and regulatory compliance for medical research studies. Our team of medical research and clinical trials experts will help guide you through the process of clinical trial design, approval, and execution.
Mission
Provide high quality clinical trial management services for the pharmaceutical and biotechnology industries, to accelerate the development of new, safe, and effective therapies. That help transform and positively impact our community by always delivering the best care to our partners and clients.
Vision
Bring life-changing therapies to our global community through liberated clinical research to help advance tomorrow’s medicine today.
Our Values
Strong Ethics Dependability, Integrity Safety Good, Clinical Practice, Commitment Compliance.
Our staff
Our research team is comprised of a certified Director Of Research, Principal Investigators, Sub-Investigators, Clinical Research Associates, Clinical Research Coordinator, Nurse, IRB Staff, and Data Management, with more than five years of experience in this field. The Principal Investigator is responsible for the management and integrity of the design, conduct, and reporting of the research project and for managing, monitoring, and ensuring the integrity of any collaborative relationships. Additionally, the Principal Investigator is responsible for the direction and oversight of compliance, financial, personnel, and other related aspects of the research project to ensure that research is conducted per GCP, SOP, and HIPAA. Clinical Research Associates are responsible for setting up, coordinating, and supervising clinical studies. They plan, prepare, and help carry out clinical trials to test new or existing investigational products.