Specifically, small-scale batches, risk assessments and process development experience and knowledge are keys to a successful scale-up strategy.
TORONTO (PRWEB) January 08, 2020
The use of spray drying to manufacture amorphous solid dispersions is continuing to grow due to the number of drug candidates exhibiting poor solubility. Apart from addressing solubility, spray drying is a reproducible processing technology that offers improved production efficiency that can potentially reduce cost and time-to-market. Phase-appropriate Quality by Design framework can increase the understanding of the interplay between the process parameters of spray drying and product quality that, when applied during scale-up, increases the chances of a successful outcome of the commercial manufacturing process.
On Tuesday, January 21, 2020 at 11am EST (4pm GMT/UK), industry experts will describe why it is essential to select a robust formulation in the early phase for easier scale-up during development and manufacturing. Specifically, small-scale batches, risk assessments and process development experience and knowledge are keys to a successful scale-up strategy.
- How to determine when spray drying is the right technology for bioavailability enhancement
- The importance of process and formulation parameters that need to be addressed for successful commercial scale-up
- The importance of the optimization of process parameters and understanding possible pitfalls during execution
- How integrated services can minimize risk and save cost and time on development and manufacturing process
For more information or to register for this event, visit Optimizing Spray Drying Strategies for Commercial Pharmaceutical Manufacturing.
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