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July 20:

Keynote
Michael Kopcha, PhD, RPh
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Introduction to the Office of Process and Facilities (OPF)
Robert Iser, MS
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Current Thinking on Microbiological Controls for Nonsterile Drug Products
Erika A. Pfeiler, PhD
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Aseptic Processing of Biological Products: Current Regulatory Issues
Candace Gomez-Broughton, PhD
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Microbiological Assessment Considerations Panel Click for Recording
Recommendations for Manufacturing Process Information in Prescription Drug Applications
Akm Khairuzzaman, PhD
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Manufacturing Process: Common Deficiencies and Recommendations for Information Request Responses
Ubrani Venkataram, PhD
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Manufacturing Process Considerations for Immediate & Modified Release Products
Rakhi B. Shah, MS, PhD
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Manufacturing Process Considerations for Lyophilized Products
Kumar Janoria, PhD
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Manufacturing Process Assessment Considerations Panel Click for Recording
Current Submissions Expectations for Facility Information
Quallyna Porte, MBA
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Lifecycle Facility Assessment
Christina Capacci-Daniel, PhD
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Facility Assessment Considerations Panel Click for Recording

July 21:

Points to Consider for the CMC Review of Therapeutic Biologics
Willie Wilson III, PhD
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Analytical Procedures and Method Validation
Lucinda (Cindy) Buhse, PhD
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Hot Topics – Drug Substance Review in CDER
M. Scott Furness, PhD
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Emerging Technology/CM
Sau (Larry) Lee, PhD
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Panel Discussion Click for Recording
Complex Drug Substances
Kshitij A. Patkar, PhD
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Risk-Based CMC Review/Quality Informatics in Knowledge Management
Andre Raw, PhD
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Application of process capability in pharmaceutical manufacturing
Alex Viehmann
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Panel Discussion Click for Recording
Post-Approval Change Management with sANDA Examples and Case Studies
Niles Ron, PhD, MBA
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Biopharmaceutics Review – Current Practices and Expectations
Tapash Ghosh, PhD
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Practical Implementation of ICH Q3D: Guideline on Elemental Impurities
John Kauffman, PhD
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Proper CMC Submission-ANDA and Content of CMC Section
Nashed Samaan, PhD
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Panel Discussion Click for Recording