C3 Research provides clinical monitoring services of high quality and value to our clients. Our monitoring tenets are founded on excellence, thoroughness, customer service, and ensuring clinical trials are monitored according to regulatory requirements. We have a staff of clinical monitors who are experienced in a variety of therapeutic indications and are available regionally within the United States and other parts of the world. We provide a team based approach which enables our monitors the ability to provide customized monitoring services to meet our clients clinical trial needs.
C3 Research utilizes technological advances to support our monitoring activities. We use a customized monitoring approach to conduct visits on-site and remotely to manage the complexities of today’s clinical trials.
C3 Research monitors are experienced in conducting site qualification visits, site initiation visit, site interim monitoring visits, and close-out visits. The monitoring team works closely with the investigative site staff as the client representative to ensure staff are trained, protocol adherence is maintained, and data critical to the clinical trial are being collected.
- Site Qualification
- Site Initiation
- Interim Monitoring
- Remote and Central Monitoring
- Unblinded Pharmacy Monitoring
- Site Closeout