Newsletter | March 12, 2025

03.12.25 -- QbD Insights And CDMO Expertise To Streamline Biologics Development

Formulation Through Manufacturing Under One Roof

Partner with a CDMO that understands the unique challenges of emerging biopharma, providing expert guidance in formulation development, manufacturing, and regulatory navigation to streamline your drug development journey.

 

Quality By Design (QbD) For Biologics From A CDMO Perspective

By adopting Quality by Design (QbD) principles in your biologics development and manufacturing process, your team can better ensure consistent product quality, mitigate risks, and optimize efficiency — aligning with patient safety and long-term commercial success.

 

QbD For Process Validation Campaigns, Commercial Manufacturing

Watch as industry-leading bioprocess experts explore the challenges and opportunities that arise when implementing QbD in biologics development and manufacturing, and gain valuable insights into how QbD principles can be applied in real-world drug product development.