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Wendy Beeby

Takeda Pharmaceuticals
Director, Clinical Document Management and Trial Support
Wendy Beeby is Director of Clinical Document Management and Inspection Readiness at Takeda, responsible for the strategic direction of clinical document management and working in collaboration with functional leads to implement effective inspection readiness and support plans. 

With a career of over 20 years working in the pharmaceutical industry, Wendy has enjoyed building customer focused teams which provide expert guidance and support on Trial Master File management and inspection preparedness.

In collaboration with TMF expert vendors, Wendy has developed innovative models for TMF quality review which can adapt quickly to fast growing organization.  Having implemented eTMF, she more recently focused on an eTMF migration solutions to support outsourced trials. Wendy has enjoyed working with core team experts in company acquisitions and has implemented strategies for the integration of clinical records, systems and teams.