Trial Agents

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EU clinical-trial operational telemetry derived from CTIS authorisations, structured as a trial-by-service-provider-by-function matrix. For each authorised trial the data resolves: whether a CRO or CRO-like provider is engaged, which provider group (IQVIA/Q² Solutions, PPD, Clario/ERT/Bioclinica, ICON, Syneos, Medidata, Parexel), the outsourced functions present across a nine-category service taxonomy (central lab/bioanalysis/PK, imaging/ECG/central reading, patient recruitment/retention/reimbursement, data management/statistics, eClinical/IRT/randomisation, supplies/logistics, monitoring/CTIS-EC support, safety/pharmacovigilance, PRO/eCOA outcomes tech), the country-participation count, site count, planned sample size, design attributes (randomised, adaptive), and recruitment channel (digital, remote support, registry/advocacy). Disease labels are normalised into indication groups. The example slice covers 247 EU neurology Phase III trials with 1,087 country participations.