Traditional drug manufacturing and drug delivery process development requires a huge time and financial investment. Pharmaceutical and biopharmaceutical leaders are leveraging the power of in silico approaches to address the unsustainable cost and time required to develop drug manufacturing, production scale up and drug delivery processes.
Applying engineering simulation and mechanistic modeling to identify the best delivery route or to scale up production equipment from lab scale to mass production is crucial to achieve regulatory approval on a sustainable timescale and budget. Simulation lowers costs while delivering a better and safer process.
Join PADT’s Senior Simulation Support & Application Engineer and pharmaceutical expert Sina Ghods for an in-depth look at challenges facing engineers working in this industry, Ansys capabilities that can provide solutions, and examples of outputs expected after implementing simulation. This presentation will focus on the following areas:
- Mixing & Scale-up
- Tablet Compaction
- Chromatography
- Democratization of Mixing Simulation
- Lyophilization
- Clean-in-Place (CIP)
- And much more
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