1 min read

Breaking Barriers: Combining Cell Line Development Innovation with Improved Process Development Workflows to Streamline Path to FIH

Learn how KBI Biopharma’s SUREtechnology Platform™, powered by Selexis®, combines refined project workflows to accelerate the development of complex biologics, from optimized cell line generation to rapid transitions to toxicology studies—all paving the way to First-in-Human trials.

 

 

Overview

This webinar focuses on how KBI Biopharma's SUREtechnology Platform™, powered by Selexis®, enables rapid advancement of new complex biologics from early development to first-in-human (FIH). Emphasizing both the speed and quality, the discussion will cover:

  • Optimized Cell Line Development: How the integration of the SUREtechnology Platform™ accelerates the creation of high-performing, stable cell lines tailored for biologics production.
  • Transposase and Versatility: Insights into the platform’s modular workflows and advanced transposase technology, which allows for highly efficient gene insertion, enabling increased clones performance consistency, further reducing cell line development bottlenecks.
  • Streamlined Path to Toxicology Studies: A step-by-step breakdown of the streamlined process that minimizes time to reach preclinical toxicology milestones, emphasizing rapid transitions from cell line development to tox studies.
  • Speed to FIH: How KBI Biopharma’s unique capabilities enable a significantly faster path to first-in-
    human studies, ensuring customers can achieve clinical milestones with confidence.

Presenters

Leslie Wolfe

Leslie Wolfe

VP of Process Development & Site Head
 
Bio Link    Linkedin Icon
Shaunak Uplekar Headshot

Shaunak Uplekar

Associate Director of Process Development
 

 

Let's Connect

Interested in learning more about KBI Biopharma? Contact us today.

 

Biosimilar Development

Biosimilar Development | Biobetters | Biosuperiors - KBI Biopharma. Visit our website or contact us to learn more.

Read More
What ASMS 2026 Is Signaling About the Future of Biologics Development

What ASMS 2026 Is Signaling About the Future of Biologics Development

Biopharma innovators must rethink CDMO strategies amid new tariffs and the BIOSECURE Act, focusing on long-term defensibility and supplier risk.

Read More
Early Microbial Protein Development Decisions That Can Cost You Later

Early Microbial Protein Development Decisions That Can Cost You Later

Biopharma innovators must rethink CDMO strategies amid new tariffs and the BIOSECURE Act, focusing on long-term defensibility and supplier risk.

Read More