Source verification of data is essential for ensuring the validity of clinical trial data. Whether you are monitoring 100% of your data for a regulated trial or a sampling for post-market trials, our monitors can help you achieve the compliance you are looking for. Our monitors, located both internally and regionally, have been trained in ICH/GCP and have extensive knowledge in medical devices across a wide range of therapeutic areas.

Monitoring Management

Symbios Clinical provides customers with one contact to report on the progress of the project and monitoring visits. By actively managing our monitors, we ensure reports are completed on time. Monitoring reports that are delayed result in lost information and the need for additional monitoring trips. Our monitors meet our customers' expectations for report turnaround every time.

Customer Service

As with all of our services, special attention to customer care is a key value for our monitors. When challenged by difficult situations, our monitors maintain professionalism and approach site personnel with respect and consideration. They are able to convey important messages, and at the same time continue to communicate effectively.