MedClinica is a Global Clinical Research Service partner, providing comprehensive Clinical Research Services for Biologics, Medical Devices, Biotech, Nutraceuticals, and Pharmaceutical companies from Phase I to Phase III and Late phase studies. MedClinica teams conduct studies in strict adherence to ICH-GCP, national & international regulations like EMA, US FDA, & DCGI, and in compliance with the protocol and other statutory legal requirements.

MedClinica provides End-to-end clinical Trials or Stand-alone like Clinical Operation, Clinical Data management, Biostats & SAS programming, Medical Writing, Pharmacovigilance, Regulatory, Quality Assurance, and end-to-end Clinical Validation Studies.

MedClinica team is the perfect blend of rich experienced professional graduates and postgraduates- MBBS, MD, Pharma D, M Pharm, & B Pharm. MedClinica delivers exceptional and customer-success-enabled services with top-notch quality supported by flexible timeframes & cost-effectiveness,

To Know more, visit www.medclinicacro.com