CliniRx services are offered through our offices and study sites across India and the United States. We offer ICH-GCP compliant clinical trials from Phase I to IV in key therapeutic areas.

CliniRx provides end to end services covering the entire spectrum of the clinical development process starting from the conduct of Feasibility Studies, Study Planning to Regulatory Submissions, Site Evaluation and Selection, Site Monitoring, Project Management, Medical Monitoring, Pharmacovigilance, Clinical Data Management, Data Analysis, Medical Writing and Quality Assurance.

CliniRx has prior, successful experience as the lead CRO for several global studies involving sites in India and Europe. CliniRx has one of the largest networks of GCP trained and compliant sites in India. Whatever the model selected by the Sponsor, agility and flexibility is the key to CliniRx’s performance. We understand every study has its own requirements; therefore, CliniRx adopts a customized approach to provide best-in-class service and support to Sponsor’s requirements.