Our team works closely with sponsors/partners to deliver the highest quality of clinical trial data. Our teams are flexible and ensure to maintain quality standards to meet the sponsor requirements for completion of assigned projects within the stipulated timelines.
We ensure the conduct of clinical study in compliance with regulatory and ICH-GCP guidelines with strict adherence to the protocol and sponsors requirement. Our clinical research services include but not limited to Site Identification, Feasibility Assessment, Pre-study Visit, Selection of ICH-GCP Trained and Qualified Investigators, Ethics Committee Submission of Study Documents and Obtaining Approvals, Site Initiation Visits, Site Monitoring, Medical Monitoring, Data Management, Site Close Out and Data Archival.