CRB subject matter experts Kim Nelson, Ph.D, director biopharmaceutical services, and Peter Walters, process engineer, are conducting an introductory webinar on “Cell Therapy Facilities—Designing for Flexibility, Scalability, and Cost Effectiveness,” including what operational, technical and support spaces are required and how Current Good Manufacturing Practice and biocontainment requirements impact design.
A key aspect that will be discussed is the identification of required Current Good Manufacturing Practice support functions and their sizes.
Attendees will also learn more about Food and Drug Administration and National Institutes of Health requirements, how to consider and address mechanical and electrical needs and how to design a facility in a cost-effective and flexible manner. General costs for cell therapy facilities will also be discussed.
The webinar is July 25, 12:00 p.m. EDT