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Utpal Munshi, Ph.D.
Division Director
US Food and Drug Administration
Poster(s):
(W1230-02-11) Risk Assessment for Extrapolation of Bioequivalence Conclusion from a Male-Only Study Population to the General Population
Wednesday, October 23, 2024
12:30 PM – 1:30 PM
MT
(M1530-04-23) Deciphering Sub-Therapeutic Risks: Integrating In Vitro Release and Modeling for Lamotrigine Extended-Release Tablets
Monday, October 21, 2024
3:30 PM – 4:30 PM
MT