Establishing a correlation between in vitro tests and in vivo product performance has always been a challenge for the pharmaceutical industry.  Without a link between specifications and in vivo performance, drug product manufacturing processes are often performed under unnecessarily tight controls. Furthermore, implementing changes post-product market approval can be challenging in a complex global environment.  This webinar will describe traditional and novel approaches towards establishing in vitro in vivo correlations. The main focus will be on solid oral dosage forms, however other dosage forms will also be discussed.

Moderators:
-Andreas Abend, Senior Principal Scientist, MSD, USA
-Horst-Dieter Friedel, FIP Chair Special Interest Group Regulatory Sciences and Quality, Germany

Panelist:
-Patrick Marroum, Senior Director in Clinical Pharmacology and Pharmacometrics AbbVie, USA