Clinical Quality Oversight has ended
avatar for Lisa D. Mulcahy

Lisa D. Mulcahy

TMF Management
Lisa Mulcahy has an extensive career in the pharmaceutical industry in the areas of Clinical Operations, Quality Management, and Clinical Documentation Management. For the past 14 years, she has focused on developing and operationalizing high-quality and compliant management processes intended to achieve complete and inspection-ready Trial Master Files (TMFs). She is experienced in performing quality and completeness reviews of study-specific TMFs.

Lisa is a co-founder and a current Steering Committee member of the volunteer team of industry representatives that created and maintain the TMF Reference Model. Lisa led the team that created and then revised the Framework for the Destruction of Paper, v2.0, that was organized and accomplished through the DRM Community.

My Speakers Sessions

Wednesday, September 29

9:30am EDT

  • Timezone
  • Filter By Date Clinical Quality Oversight Sep 27 -29, 2021
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  • General Session - Live Streamed to Virtual Audience
  • Interactive Workshop - In-Person Only
  • Networking!
  • Track A - In-Person Only
  • Track B - In-Person Only