Revolutionizing CMC in Drug Development: How to Reduce Errors and Delays in Quality by Design

Margarida Ventura (Senior Consultant) will present the webinar Revolutionizing CMC in Drug Development: How to Reduce Errors and Delays in Quality by Design on May 28, at 8:00 AM EDT. There is a second session at 12:00 PM EDT.

Quality by Design in pharma offers significant potential—but many organizations struggle to implement QbD effectively.

In this webinar, you’ll explore common mistakes that hinder QbD success—such as inconsistent risk evaluations, fragmented data sources, version control issues, and insufficient cross-functional collaboration. You’ll also hear case studies that show how  companies are transitioning from disconnected tools to completely integrated digital platforms that support more robust CMC manufacturing.  

Whether you’re at the beginning of your QbD journey or working to refine existing practices, you’ll come away with useful strategies, practical insights, and digital approaches that enable more effective and sustainable implementation. 

Even if you are not able to attend the live event, we still recommend registering in order to receive a link to the full recording.

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