DSP Clinical, a full-service CRO managing Phase I to IV clinical trials across many therapeutic areas including infertility, endocrinology, urology, and gastrointestinal studies, announced a new co-monitoring service that provides flexible, cost-effective monitoring support to help clinical trials meet study timelines.
The service, which scales to fit the size, complexity, and speed of Phase I–IV research clinical trials in any therapeutic area, can provide back-up monitors who are trained and ready to help. DSP monitors are long-term CCRA-certified employees who are fluent in a variety of EDC systems.
Sponsors can elect to have full- or part-time monitoring help with tasks such as reviewing data, conducting pre-study visits, or preparing for site audits. DSP’s monitors step in as needed, working as an extension of the existing study team while minimizing overhead and lag time. The service is available immediately.
