Monitoring is not just mandatory according to ICH-GCP, accurate monitoring is crucial in the process of producing reliable data in due time. The easiest way to achieve effective monitoring is to establish a profound cooperation with the investigators. That is exactly what our CRAs do: they consider themselves partners and not mere supervisors.

IFE Baltic is proud to have one of the best-qualified monitoring teams in Eastern Europe. They understand both the practice of medicine and of the practitioner, allowing them to work on an equal footing with investigators and coordinators alike. Working in tandem with the site, IFE Baltic CRAs establish systems and strategies that streamline the clinical trial process.

IFE Baltic CRAs conduct field and remote monitoring to ensure protocol and regulatory compliance and timely submission of high-quality data. Monitoring activities include clinical site qualification, initiation, routine monitoring, close-out, and project management. All IFE Baltic monitors are thoroughly trained in ICH-GCP and site management techniques. We eagerly embrace the latest technology-based solutions including electronic data capture, remote monitoring and data entry, and web-based clinical trial management.