@article{1442748,
      note = {Includes index.},
      author = {Gee, Adrian P.,},
      url = {http://library.usi.edu/record/1442748},
      title = {Cell therapy : cGMP facilities and manufacturing /},
      abstract = {This new edition presents a fully-updated and expanded  look at current Good Manufacturing Practice (cGMP) for cell  therapy products. It provides a complete discussion of  facility design and operation including details specific to  cord blood banking, cell processing, vector production and  qualification of a new facility. Several chapters cover  facility infrastructure including cleaning and maintenance,  vendor qualification, writing a Standard Operating  Procedure, staff training, and process validation. The  detailed and invaluable product information covers topics  like labelling, release and administration, transportation  and shipment, et al. Further chapters cover relevant topics  like writing and maintaining investigational new drug  applications, support opportunities in North America and  the European Union, commercial cell processing and quality  testing services, and financial considerations for academic  GMP facilities. A chapter on future directions rounds out  Cell Therapy: cGMP Facilities and Manufacturing making it  essential reading for any cell therapy professional  involved in the development, use, or management of this  type of facility.},
      doi = {https://doi.org/10.1007/978-3-030-75537-9},
      recid = {1442748},
      pages = {1 online resource (x, 692 pages) :},
}