Overview to Panel Discussion 20of27 Generic Drugs Forum 2018
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Keynote Address by Dr. Uhl (1of27) Generic Drugs Forum 2018
Electronic Submissions (7of27) Generic Drugs Forum 2018
Questions and Panel Discussion (20of39) Complex Generics 2018
Keynote – Office of Generic Drugs (1/28) Generic Drugs Forum 2017
Drug Substance Review - ANDA (22/28) Generic Drugs Forum 2017
Drug Substance Quality Assessment: Best Practices (23of27) Generic Drugs Forum 2018
Panel Discussion (19/28) Generic Drugs Forum 2017
GDUFA II – Review Timelines (14of27) Generic Drugs Forum 2018
Microbiology Quality Assessment (18of27) Generic Drugs Forum 2018
Panel Discussion
Integrated Quality Assessment Process (19of27) Generic Drugs Forum 2018
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Last Updated: October 3, 2026
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Summary
Presenters Khanna, Bearr, Shen, Smith, Munshi, Patel, Mbi, Sansone, Julia Lee, and Andrea Bautista answer audience questions. Presenters Sherwood, Chazin, Hasselbalch, Bercu, Andre, Resnick and Kurtz respond to audience questions. Learn more at ... Presenters Friedman, Shen, Tyner, Andre, and Kendra Stewart respond to audience questions. Learn more at ... Presenters Ryan, Jao, Rodriguez, Anh Bui, Nguyen, Randad, Berendt, and Parks respond to audience questions. Learn more at ... CDER's Jonathan Resnick covers points to consider when preparing an eCTD submission and sending to FDA. Learn more at ... Presenters respond to audience questions. ----------------------------- FDA CDER's Small Business and Industry Assistance (SBIA) ... Kathleen Uhl, MD, Director, Office of Presenters Lee, Chandra, Ghodasara, Kimble-Vance, Jiang, Kim, Spagnola, and Golson respond to audience questions. CDER's Vincent Sansone provides an overview of GDUFA II goal dates and how they are applied to original applications, ... Elizabeth Bearr from CDER's Office of Office of Howard Chazin, Linda Forsyth, Lauren Gilles, Niles Ron, and Debra Catterson
Panel Discussion 20of27 Generic Drugs Forum 2018.pdf
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