IQVAMED assists CRO/Sponsor’s outsourced clinical trials by Experienced and dedicated Clinical Research coordinator (CRC) at the site as per specified therapeutics areas of assigned Protocol under the direction of the clinical investigators. Our extremely competent CRCs handles the bulk of daily clinical trial activities and plays a critical role in study conduct. IQVAMED offer training opportunities for CRCs, both through the formal presentation and the informal interactions with the sponsor’s Clinical Research Associate (CRAs) and other highly experienced clinical research professionals as per specialized therapeutics sound to study execution at the sites.

Our experienced research coordinators offer diverse capabilities to ensure each clinical trial is conducted at the sites as per ICH-GCP in accordance with the ethical principles that have their origin in the Declaration of Helsinki, and that are consistent with the Good Clinical Practice (GCP) and the applicable regulatory requirement(s) or New Drugs and Clinical Trials Rules-2019.