In vitro dissolution testing, if reflective of in vivo drug release/absorption, is considered a surrogate for in vivo drug performance. Establishing in vitro–in vivo link to ensure clinical performance is feasible by implementing PBBM to guide product development and regulatory submissions [1].
By Jasmina Novakovic
2019 AAPS Annual Meeting PharmSci 360, November 3-6, 2019, San Antonio, Texas
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