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Harrington, Rachel

U.S. FDA
Inspection-Based Live Q&A
Rachel Harrington
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Inspection-Based Panel Discussion
Rachel Harrington
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Hartsock, Sharyl

Eli Lilly and Company
C5: All That Data…Now What?
Sharyl Hartsock
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Live Q&A (C5)
Sharyl Hartsock
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Henrici, Kir

The Henrici Group
Forthcoming PDA Technical Report on Utilizing the Quality Management System to assure Data Integrity
Kir Henrici
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Live Q&A (C5)
Kir Henrici
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Higgins, Brooke

U.S. FDA
Hot Topics and Regulatory Expectations in Aseptic Processing
Brooke Higgins
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Live Q&A (B5)
Brooke Higgins
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Hotez, Peter

Baylor College of Medicine
Live Q&A (P6)
Peter Hotez
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Vaccine Diplomacy in a Time of Doubt in Science
Peter Hotez
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Huffman, Laura

U.S. FDA
Inspection-Based Live Q&A
Laura Huffman
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Inspection-Based Panel Discussion
Laura Huffman
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Hughes, Patricia

U.S. FDA
A5: Aging Facilities vs. Modern Facilities
Patricia Hughes
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C2: Drug Quality Lifecycle: Current Regulatory Concerns
Patricia Hughes
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Live Q&A (A5)
Patricia Hughes
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Live Q&A (C2)
Patricia Hughes
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Live Q&A (ST6)
Patricia Hughes
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Review-Based Live Q&A
Patricia Hughes
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Review-Based Panel Discussion
Patricia Hughes
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Risk Management of Non-Ingredient Suppliers: Current Regulatory Concerns
Patricia Hughes
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Hutchens, Clarice

Pfizer
B4: ICH’s Initiatives to Advance Global Harmonization, Innovation, and Continual Improvement Throughout Lifecycle
Clarice Hutchens
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Live Q&A (B4)
Clarice Hutchens
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Live Q&A (ST2)
Clarice Hutchens
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Special Topic 2: Quality Management Maturity (QMM) and Metrics: What Does the Future Hold?
Clarice Hutchens
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Huynh, Mai

U.S. FDA
Inspection-Based Live Q&A
Mai Huynh
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Inspection-Based Panel Discussion
Mai Huynh
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Live Q&A (ST6)
Mai Huynh
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Special Topic 6: Risk Management of Non-Ingredient Suppliers
Mai Huynh
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