In this segment, TF Pharma's Robert Goldman talks about different views of what eSource is and how, in some instances, this clinical trial technology doesn’t save any time over using paper.
Life sciences companies are grappling with a deluge of data. Yet, strategic data management outsourcing offers potential benefits amidst regulatory and interoperability hurdles.
Electronic consent promotes better trial experiences, but many sites and sponsors are wary of giving up paper-based processes. Consider their reasons for caution and how teams can prepare for the switch.
Digital tools like ePRO and eConsent are essential in addressing pediatric trial challenges such as the diverse participant ages and family involvement, which impact retention and data quality.
As part of an expansion project, a large multinational pharmaceutical company sought a partner to simplify the payment and travel processes, improving their patients' experience.
See how improvements made to SIP have allowed for quick access to study documents and bulk actions for streamlined document management and enhanced user experience.
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