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Business & Regulation Advanced Medicine, Bioprocessing - Upstream & Downstream, Standards & Regulation

Cell Therapy Facilities – Designing for Flexibility, Scalability, and Cost Effectiveness

sponsored by CRB

The webinar will provide an introduction to the design issues for Cell Therapy Facilities. Specifically what operational, technical and support spaces are required, and how GMP and biocontainment requirements impact their design. An important aspect of this is the identification of required GMP support functions and their sizes. Mechanical and electrical needs are considered and how to address. This webinar will introduce FDA and NIH requirements, and how to design to them in a cost effective and flexible manner. General costs for Cell Therapy facilities will also be discussed.

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