IQVAMED Provides a comprehensive clinical trial monitoring service at the Investigator sites through experienced and competent Clinical Research Associates (CRAs) from feasibility to closeout with the utmost efficiency. Our CRAs is the primary point of communication between the site personals (CRCs/PI, & Co-I) and the Project Manager of the allocated study.

Our clinical monitors keep track of your study's progress to verify that it is conducted and recorded in accordance with your protocol that allows its accurate reporting, interpretation,and verification.