Optimized study design, precise site selection and faster patient search and identification for clinical research - in real time.
The viability of a study protocol is often assessed against historical databases that are highly aggregated and rarely up-to-date. Clinerion's Protocol Designer enables sponsors and investigators to validate and optimize their protocols based on actual, real-time patient data on a hospital, regional, national or international level. Clinerion can provide real-time access to millions of EHRs – a figure which is constantly increasing.
Protocol Designer enables protocol definition with five dimensions of query, combining criteria based on coded information (for diagnoses, treatments, medications, etc.), data (e.g. demographics, lab values) and free text (such as narratives and reports), and an unlimited number of criteria. Eligibility criteria can be mapped between all standard medical and hospital-specific terminologies; free text is screened with the support of a natural language processing technologies.
Benefits of the Protocol Designer:
|To clinical trial sponsors:||
|To physicians and hospitals:||