GCRS acts as a common platform between the Principal Investigator(s) and Sponsor(s)/CRO(s) for the triumphant execution of clinical trials. In the span of six years we have successfully completed more than 150 studies with track record of exceeding enrollment goals for many of our clinical trials. Our team brings more than 150 years of collective experience in clinical research.
Our highly competent Project Management Team and Clinical Research Coordinators at each study site assist and support the investigators with all study related activities, ensure compliance with applicable regulations, ICH-GCP guidelines and efficient completion of assigned duties. Our CRCs have adequate operational knowledge of the research process, strong personal ethics and clinical competency.
GCRS claim strict adherence to protocol, compliance to regulatory norms, extensive documentation, absolute accuracy, an ethically sound patient recruitment strategy, and efficient site management through our well laid Site Management specific Standard Operating procedures (SOPs).
GCRS strength is well trained, experienced professionals who have knowledge and experience in clinical operations, across various therapeutic groups and indications. Therapeutic Specialties: Oncology, CNS, Cardiovascular, Diabetes and Endocrinology, Vaccines and Biologics. Gastroenterology, Spine Management, Pain / Inflammation, Nephrology, Urology, Orthopaedics, Obstetrics and Gynaecology, Medical Devices & Diagnostic Trials, Immunology
Founded in 2006 and headquartered in Hyderabad, Gleneagles Global Clinical Research Services (GCRS) is a comprehensive site management organization serving the biopharmaceutical and medical -device industry. Our mission has been, and will always be quality. We strive to lead the world in the diagnosis and treatment of disease and to train tomorrow's great doctors and nurses. Above all, we aim to provide the highest quality health-care services to all of our patients.
From escalating the span of our business to positioning our company ahead of competition in the SMO segment, we have emerged as the premium "Multi-site, Multi-specialty SMO" offering cost effective and competent clinical trial execution.Our business practices are consistent with the Code of Ethics, Patient care, Strict Regulations and Timelines.