Process Development and Technical Operations Manager
Senior Business Development Manager
Technical and Regulatory Advisor
Originally Aired: January 31, 2024
Time: 8:00 am PT, 11:00 am ET, 17:00 CET
In drug manufacturing, aseptic filling is the crucial final step in advancing biologics candidates into the clinic. Whether drug manufacturers outsource the process to a CDMO or bring the filling operations in-house, it is important to implement effective techniques and processes that minimize contamination risks and human error while meeting the strictest compliance standards.
In this GEN webinar, our speakers will describe best practices and tools that biomanufacturers can adopt to optimize their aseptic filling processes. They will share examples of effective aseptic filling operations that leverage automation and robotics to safely package drug products. Topics covered in the webinar will include:
- How a fully isolated robotic filling system helps reduce risk in filling high-value drug products
- Commonly asked questions around inspections and regulatory compliance
- Impact of aseptic filling technology on key quality and performance metrics
- Benefits of collaboration among end users, enabled by the standardized equipment design
A live Q&A session followed the presentation, offering a chance to pose questions to our expert panelists.
Produced with support from: