Sponsors and even CROs often struggle to capture capture certification and qualification from clinical site personnel.
UL’s Clinical Site Qualification Solution ensures higher quality during the trial, and also reduces the time spent on site initiation and site certification, by delivering and capturing both protocol and non-protocol activities based on each person’s role in the study.
You can also capture investigator meetings via video to deliver at a later date, and also share supplementary material following the site initiation phase.
Importantly, the functionality in ComplianceWire ensures that study managers only gain reporting visibility into the site individual based on a specific site, study, role and region, even if that individual is involved in multiple studies.
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