Our Clinical Research Associates (CRAs) team has an extensive experience in supporting
the clinical trials through the monitoring surveillance activities customized to your research study
requirements to ensure adequate protection of the rights and safety of all human subjects involved in your study.
Our CRAs are highly trained in the broad aspect of the clinical study phases, and not limited to, site selection, site qualification, development of plans, site personnel training, study conduct, source data verification, database lock, maintenance of documentation, and study closure. Our team specializes in remote, on-site and centralized monitoring visits based on the trial requirements. They are experienced in Clinical Trial Management Systems, EDC systems, and Trial Master Files. The MHICC monitoring team ensures that the quality and integrity of the reporting clinical data are in accordance with the protocol, relevant Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), applicable regulatory authorities’ requirements and that they are verifiable from source documents.