Behind the Curtain: Sterile Filling Readiness in the Drug Device Delivery Ecosystem

Go behind the curtain as we delve into sterile filling equipment readiness and its crucial role in the drug delivery innovation ecosystem. Understanding the collaboration between Contract Development and Manufacturing Organizations (CDMOs) and their equipment vendors is essential for ensuring successful and timely product delivery. Our expert panel, featuring representatives from Bausch+Stroebel, SKAN, and Grand River Aseptic Manufacturing, will discuss how sterile filling equipment adapts to variations in drug delivery systems while maintaining compliance with regulatory requirements.

 Key topics include: 

• The journey from concept to reality: What happens when custom components are involved?
• Overcoming challenges: Insights into using novel components and ensuring smooth operations across technologies.
• Adhering to regulatory standards: Maintaining Annex 1 compliance amidst flexible equipment and shifting industry demands.
• Unique capabilities of CDMOs: Why their investments in filling lines for syringes and cartridges position them as leaders in the market.

Whether you’re a pharmaceutical or biotech professional looking to enhance your understanding of the filling process or seeking strategies to impact your product’s success, this webinar is tailored for you. Don’t miss this opportunity to go behind the scenes with industry leaders and gain valuable insights on the CDMO’s role in device delivery ecosystems.

Speakers:

• Mary Lou Glotzbach – Sr. Manager, Drug Delivery Partnerships, Grand River Aseptic Manufacturing
• Andre Zdunczyk – North American Sales/Business Development & Marketing Director, Bausch+Stroebel
• Adrian Keller – Strategic Product Manager, SKAN