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  • Dr. Michael Braun
  • Director Late Stage Drug Product Development
  • Boehringer Ingelheim Pharma, Germany
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Key Topics

Meaningful application of PATs

Common Scale-up issues and troubleshooting

Integrating material science concepts in drug product development to simplify formulation and speed up process development

Application of stability simulations to identify shelf life-limiting Quality Attributes and complement real time stability studies

Takeaways & Special features

Understand
industry approaches for scaling-up dosage forms applying QbD principles

Learn
How to translate theoretical scale-up and current regulatory guidance into practice - What is really relevant?

Gain
Knowledge of formulation, process transfer and validation for commercial drug production. 

Delegate Fee

from 1798 € Buy

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Based on your requirements, we will build a practical training including content tailored to your specific needs, our cutting edge methodologies and relevant modules from our training portfolio.

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