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A recent IQVIA survey revealed that one-third of sponsors fully or partially outsource their clinical trials to several service providers (i.e., CROs, etc.). Although this model usually results in the successful execution of trials, it also creates numerous challenges.

For example, sponsor’s data resides with different providers and reports and metrics are produced at varying frequencies and provided in different formats and nomenclatures. This requires sponsors to spend too much time wrangling data from all trials across their portfolio and manually processing reports to maintain the necessary, and ICH E6 required, level of operational oversight.

Join this webinar to learn how IQVIA Technologies Clinical Data Analytics Solutions (CDAS) offers sponsors an answer to the challenge of high quality, timely oversight in an outsourced clinical trial model.

• Review the regulatory requirements and subsequent challenges of maintaining high quality sponsor oversight in an outsourced trial model.
• Learn how IQVIA’s CDAS technology and services can provide an efficient path to consolidating and harmonizing data across any provider source.
• Learn about the value of analytics delivered via standard dashboards, self-service reporting capabilities, and innovative generative AI chat features.

Speakers:

Wendy Morahan
Sr. Director, Product, CDAS, IQVIA Technologies

Rathipriya Bhaskar
Sr. Product Manager, Clinical Data Analytics, IQVIA Technologies

Prashant Bomireddipalli
Director, CDAS – Data Services, IQVIA Technologies