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Webinar

Optimizing micronization and achieving high yields from clinical to commercial

9 April 2025

2:00pm

Gain expert insight into optimizing pharmaceutical micronization while maintaining product quality, optimizing yield, and controlling the cost of goods from formulation through commercial supply.

Micronization plays a crucial role in enhancing the efficacy and bioavailability of active pharmaceutical ingredients (APIs), a cornerstone of modern drug development. As drug formulations become increasingly sophisticated, achieving precise and, crucially, repeatable particle size control during the micronization process is absolutely critical. This level of control is essential not only for ensuring optimal drug performance in terms of absorption, distribution, metabolism, and excretion but also for robust and reliable manufacturability. Inadequate particle size control can lead to inconsistent drug delivery, impacting therapeutic outcomes and potentially causing adverse effects. And it can create significant challenges in the manufacturing process, affecting everything from flowability and compressibility to stability and shelf-life. 

This comprehensive webinar will delve into best practices for optimizing the micronization process, all the way through to full-scale commercial production. Our panel of expert speakers will share their insights and practical experience on a range of key topics. They will discuss the critical considerations involved in selecting the most appropriate milling equipment for specific API characteristics and target particle size distributions.  

The webinar will also cover the refinement of critical process parameters, including milling speed, feed rate, grinding media selection, and temperature control, emphasizing the importance of a data-driven approach to optimization. Furthermore, attendees will learn about effective strategies for maximizing product yield while simultaneously improving cost efficiency, a vital consideration in today’s competitive pharmaceutical landscape. This includes exploring techniques for minimizing API loss during processing and optimizing energy consumption. 

Join us for an in-depth discussion on how the strategic combination of cutting-edge technology and specialized expertise can help overcome the multifaceted challenges inherent in drug development. This webinar will empower you to successfully scale API particle engineering while consistently maintaining product quality, optimizing yield, and effectively controlling the cost of goods from initial formulation through to commercial supply.  

Key learning points: 

  • Understand the key advantages of micronization as a particle engineering technique 
  • Explore solutions to scale, yield, and COGS for API particle engineering  
  • Learn strategies for optimizing micronization from clinical to commercial scale 

Don’t miss this opportunity to gain valuable insights and enhance your understanding of this critical process. 

REGISTER A PLACE NOW >>> 

FAQs

FAQs 

Is the panel discussion free? 

Yes – there is no charge to watch the panel discussion, either live or on-demand. 

When will the panel discussion take place? 

09 April at 3pm BST. 

Can I watch it later? 

The panel discussion will become available to watch on-demand shortly after the live webinar takes place. 

What are the benefits of attending live? 

You’ll be able to ask the speakers your questions, which will be answered live in the Q&A towards the end of the session. 

How long will the panel discussion be? 

This panel discussion will last up to an hour. 

What do I need to watch this panel discussion? 

All you need is a computer with an internet connection. We recommend using headphones if possible if you’re in an office environment.