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Thursday, January 23 • 3:15pm - 4:00pm
Review Draft ICH E8 Considerations For Clinical Studies

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  • Describe the proposed stakeholder role (including patients and treating physicians) proposed in designing clinical trials
  • Explore what the proposed ICH guideline means for subjects in clinical trials
  • Understand how designing quality into a study can increase the trust in the results

Speakers
avatar for Matt Lowery, ACRP-CP, CCRC

Matt Lowery, ACRP-CP, CCRC

Director of Clinical Research, Suncoast Neuroscience Associates
Matt has over 12 years of experience in clinical research on both the site and sponsor level. On the site side, Matt has worked as a study coordinator, site manager, director of clinical research, and assists other sites with general consulting, business development, and budget/contract... Read More →
avatar for Betsy Fallen

Betsy Fallen

Consultant, BAFallen Consulting LLC
Ms. Fallen is an authority on the business processes and associated use of information technology in drug development with a focus on regulatory and clinical. A passionate advocate for moving life sciences business on-line, Betsy is an expert on regulatory and clinical operations... Read More →


Thursday January 23, 2020 3:15pm - 4:00pm