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Based on innovative tablet technology, premierConsent® will – for the first time – combine patient education using custom-tailored multimedia content on the one hand and informed consent process capturing using audiovisual recordings on the other hand. premierConsent® will serve as a clinical trial information hub for clinical monitors, institutional review boards, ethics commissions, regulatory authorities, and trial sponsors, with varying levels of access and information detail depending on applicable regulations. Additionally, premierConsent® will eliminate the need for paper documents and significantly impact and enhance clinical trial safety, data reliability, regulatory compliance and cost efficiency.