Event / Webinar

Improving Sponsor Oversight of the Trial Master File at Chiesi: A Case Study

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Speakers

Marisa Minetti

Head of Late Phase Clinical Trial Administration, Chiesi Group

Jenny Zecchini

Clinical Research Department Director, CROMSOURCE

Rob Jones

Director, Professional Services, Phlexglobal

Regulators have made it abundantly clear - through recent guidance and inspection findings - that demonstrating sponsor oversight of an outsourced study is a critical requirement for TMF health and inspection-readiness. Watch this webinar to discover how global biopharmaceutical company Chiesi and its CRO partners collaborate to ensure ongoing oversight compliance, in the face of increasing documentation requirements and trial complexity.

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