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.
Marisa Minetti
Head of Late Phase Clinical Trial Administration
Chiesi Group
Jenny Zecchini
Clinical Research Department Director
CROMSOURCE
Rob Jones
Director, Professional Services
Phlexglobal