SEP 22, 2021 8:00 AM PDT

Cell therapy needs a data-driven and certified cleanroom-compatible CO₂ incubator

Speaker

Abstract
Date:  September 22, 2021
Time: 8:00am (PDT),  11:00am (EDT)
 
New technologies generating successful cell and gene therapy approaches have contributed to a global growth of institutions that cultivate stem cells, T cells and other primary cell types under stringent conditions. These cells are exquisitely reactive to their environment and challenging to manage. For any therapeutic designed for use in a human patient, careful safeguards are inherent to the development and production. Good manufacturing practices (GMP) must be followed. As part of GMP, working in a cleanroom setting helps to produce a therapy which is safe and effective, pure, and of high quality. Culturing cells in a cleanroom under GMP comes with new challenges, and require a CO incubator that can help meet these challenges by reducing risk to the therapy, including features to control particulates and contamination, compatibility with enhanced cleaning procedures, documentation to support validation processes and certification for ISO Class 5 and Grade A/B use in accordance with ISO 14644-1.
 
Learning Objectives
  • Review the global increase in cell and gene therapy applications
  • Describe the needs for cleanroom equipment
  • Explore attributes and certifications that make a CO incubator compatible for cleanroom work
  • Demonstrate that incubator performance can vary and how the parameters affect cultured cells
 
 
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LabRoots is approved as a provider of continuing education programs in the clinical laboratory sciences by the ASCLS P.A.C.E. ® Program. By attending this webinar, you can earn 1 Continuing Education credit once you have viewed the webinar in its entirety.

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