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Industry Event

Scope Summit 2020

TransCelerate BioPharma will be in attendance and represented by the following speakers:

Tuesday, February 18

  • 12:05 PM: Change Management Clinical Supply Chain Considerations for Digitally Enabled Patient-Centric Clinical Trials, Matthew Moyer (Merck)

Wednesday, February 19

  • 11:35 AM: An Exploration of Effective Regulator Engagement Regarding the Use of Digital Endpoints Suraj Ramachandran (Merck)
  • 2:20 PM Strengthening Your Clinical QMS: A Focus on Clinical Development Processes and Associated Documentation and Training, Odette Anyangwe (Roche)
  • 2:24 PM: The Application of Quality Tolerance Limits (QTLs) as Described in ICH E6 R2, Ruma Bhagat (Genetech)
  • 4:25 PM: How Can We Improve the Patient Experience in Clinical Trials? T.J. Sharpe; Michele Teufel (AstraZeneca)

Thursday, February 20

  • 8:25 AM: Engaging with Patients in Design and Execution of Trials: Ways to Make Clinical Trials More Patient-Centric, David Leventhal (Pfizer)
  • 9:05 AM: Quality Risk Management Framework: Guidance for Successful Implementation of Risk Management in Clinical Development, Allan Chow (Amgen)

Friday, February 21

  • 9:35 AM: The Application of Intelligent Automation Technologies in Pharmacovigilance,
    Robert Taylor (Merck)
  • 11:00 AM: Assessing Your Clinical Quality Management System: A Comprehensive Review of TransCelerate’s CQMS Assessment Tool, Janis Little (Allergan)
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