MedSource Clinical Monitoring Services
MedSource is proud to offer one of the finest clinical monitoring teams in the industry to ensure protocol and regulatory compliance as well as timely submission of high-quality data. Our regional CRAs educational backgrounds range from Registered Nurses to MD’s - bringing to our Sponsor a vast therapeutic background and experience. Each monitor is experienced and trained in FDA regulations, ICH guidelines, and GCP compliance.
Because Clinical Monitoring is the “backbone” of our business model, with confidence we can state:
- Our expertise in clinical research monitoring means our query rates are consistently lower than the industry average. This level of excellence provides greater accessibility to key information required in making timely critical drug development decisions.
- Our clinical research associates average over thirteen years of monitoring experience, with the majority in CNS, oncology and infectious diseases.
- Our monitors can directly participate in data management processes, therefore promoting closer integration between data management and site activities, resulting in higher-quality clinical data throughout the entire process.
- Because our monitors are working within their chosen therapeutic areas, we retain an established group of experienced monitors who evolve long-standing relationships with our investigative sites.