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Clariness (ClinSight) — Operational clinical trial recruitment and feasibility corpus, accumulated across 20 years: ~2,500 studies with ~1 million patients, capturing country- and site-level enrolment performance over time, screen-failure and eligibility-criteria outcomes, protocol-burden effects on patients and sites, start-up timelines and the impact of specific protocol design choices on recruitment. Combined with external real-world datasets to benchmark and model protocol feasibility. Mid-size European specialist with an outsized data asset: ~180 employees, ~$39M revenue, Hamburg headqua…
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Operational clinical trial recruitment and feasibility corpus, accumulated across 20 years: ~2,500 studies with ~1 million patients, capturing country- and site-level enrolment performance over time, screen-failure and eligibility-criteria outcomes, protocol-burden effects on patients and sites, start-up timelines and the impact of specific protocol design choices on recruitment. Combined with external real-world datasets to benchmark and model protocol feasibility
Scale Stated directly: ~2From 20 yearsCoverage Health Care
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Clariness (ClinSight) — Operational clinical trial recruitment and feasibility corpus, accumulated across 20 years: ~2,500 studies with ~1 million patients, capturing country- and site-level enrolment performance over time, screen-failure and eligibility-criteria outcomes, protocol-burden effects on patients and sites, start-up timelines and the impact of specific protocol design choices on recruitment. Combined with external real-world datasets to benchmark and model protocol feasibility. Mid-size European specialist with an outsized data asset: ~180 employees, ~$39M revenue, Hamburg headqua…
Clariness (ClinSight) offers (Alternative, Reference, Fundamental) — Stated directly: ~2,500 clinical studies and ~1 million patients of recruitment and feasibility data spanning 20 years, augmented with external real-world datasets. This is a compact but extremely dense corpus — the value is in the labelled study-outcome pairs, not raw record volume.
Enrolment-velocity forecasting and feasibility assessment at protocol design; eligibility-criteria optimisation to reduce screen failure; protocol-burden reduction (visit and procedure load) informed by observed effects; country and site selection strategy; recruitment-timeline benchmarking for sponsors, CROs and procurement teams; and for a buyer building trial-operations models, a rare labelled corpus of protocol design choices paired with realised operational outcomes across 2,500 studies
The data is with 20 years of history.
Coverage spans US, Europe; Pharmaceuticals; alternative, reference, fundamental; equities.
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