This webinar will delve into the challenges of translating workflows into a GMP-compliant environment, specifically focusing on regenerative medicine in cardiovascular diseases. Discussion will focus on the pre-clinical development path, and hurdles related to raw materials supply chain management, and identifying equipment compatible with the execution of novel, compliant manufacturing processes.
Learn how the MACSQuant® Tyto®, with its closed and sterile cell sorting system, is the ideal solution for easily translating workflows from the research bench to clinical manufacturing.
Attend this webinar to learn about: