Q Founder Series | Designing Quality and ICH Compliance into Clinical Trials

Join us as we learn about the complex drug development journey from the initial discovery of therapeutic targets to preclinical research and the clinical research phases.  This presentation will share how to proactively build quality, patient safety, and data integrity into clinical trial planning and conduct from a multiple stakeholder perspective. 

SPEAKER BIO:

Kathleen Wisemandle

Founder | Strategic Advisor and Executive Coach | Aspire To Grow Consulting

Kathleen has 30+ years in the Biopharma space and has been involved in a range of critical R&D areas, including IND planning, protocol development, operational planning, team development and comprehensive risk identification and mitigation planning, with a particular focus on optimizing vendor selection, managing Key Opinion Leaders (KOLs), and ensuring regulatory compliance.

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