Your browser doesn't support javascript.
loading
End-to-end collaboration to transform biopharmaceutical development and manufacturing.
Erickson, John; Baker, Jeffrey; Barrett, Shawn; Brady, Ciaran; Brower, Mark; Carbonell, Ruben; Charlebois, Tim; Coffman, Jon; Connell-Crowley, Lisa; Coolbaugh, Michael; Fallon, Eric; Garr, Eric; Gillespie, Christopher; Hart, Roger; Haug, Allison; Nyberg, Gregg; Phillips, Michael; Pollard, David; Qadan, Maen; Ramos, Irina; Rogers, Kelley; Schaefer, Gene; Walther, Jason; Lee, Kelvin.
Afiliación
  • Erickson J; National Institute for Innovation in Manufacturing Biopharmaceuticals, Newark, Delaware, USA.
  • Baker J; Office of Biotechnology Products (OBP), Center for Drug Evaluation and Research (CDER), U.S. Food and Drug Administration, Silver Spring, Maryland, USA.
  • Barrett S; Global CMC Development, Sanofi, Framingham, Massachusetts, USA.
  • Brady C; Biologics MS&T, Bristol-Myers Squibb, Devens, Massachusetts, USA.
  • Brower M; Biologics Process Research and Development, Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Carbonell R; National Institute for Innovation in Manufacturing Biopharmaceuticals, Raleigh, North Carolina, USA.
  • Charlebois T; BioTx Pharmaceutical Sciences, Pfizer, Andover, Massachusetts, USA.
  • Coffman J; Biopharmaceutical Development, AstraZeneca, Gaithersburg, Maryland, USA.
  • Connell-Crowley L; Process Design, Just-Evotec Biologics, Seattle, Washington, USA.
  • Coolbaugh M; Global CMC Development, Sanofi, Framingham, Massachusetts, USA.
  • Fallon E; Manufacturing Science and Technology, Drug Substance, Genentech, Inc., Oceanside, California, USA.
  • Garr E; Biologics MS&T, Bristol-Myers Squibb, Devens, Massachusetts, USA.
  • Gillespie C; Biologics Process Research and Development, Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Hart R; Process Development, Amgen, Cambridge, Massachusetts, USA.
  • Haug A; National Institute for Innovation in Manufacturing Biopharmaceuticals, Newark, Delaware, USA.
  • Nyberg G; Biologics Process Research and Development, Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Phillips M; Next Generation Processing R&D, MilliporeSigma, Bedford, Massachusetts, USA.
  • Pollard D; Sartorius Corporate Research, Sartorius, Boston, Massachusetts, USA.
  • Qadan M; Biologics Research and Development, Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Ramos I; Biopharmaceutical Development, AstraZeneca, Gaithersburg, Maryland, USA.
  • Rogers K; Material Measurement Laboratory and Office of Advanced Manufacturing, National Institute of Standards and Technology, Gaithersburg, Maryland, USA.
  • Schaefer G; API Large Molecule BioTherapeutics Development, Janssen R&D, Malvern, Pennsylvania, USA.
  • Walther J; Global CMC Development, Sanofi, Framingham, Massachusetts, USA.
  • Lee K; National Institute for Innovation in Manufacturing Biopharmaceuticals, Newark, Delaware, USA.
Biotechnol Bioeng ; 118(9): 3302-3312, 2021 09.
Article en En | MEDLINE | ID: mdl-33480041
An ambitious 10-year collaborative program is described to invent, design, demonstrate, and support commercialization of integrated biopharmaceutical manufacturing technology intended to transform the industry. Our goal is to enable improved control, robustness, and security of supply, dramatically reduced capital and operating cost, flexibility to supply an extremely diverse and changing portfolio of products in the face of uncertainty and changing demand, and faster product development and supply chain velocity, with sustainable raw materials, components, and energy use. The program is organized into workstreams focused on end-to-end control strategy, equipment flexibility, next generation technology, sustainability, and a physical test bed to evaluate and demonstrate the technologies that are developed. The elements of the program are synergistic. For example, process intensification results in cost reduction as well as increased sustainability. Improved robustness leads to less inventory, which improves costs and supply chain velocity. Flexibility allows more products to be consolidated into fewer factories, reduces the need for new facilities, simplifies the acquisition of additional capacity if needed, and reduces changeover time, which improves cost and velocity. The program incorporates both drug substance and drug product manufacturing, but this paper will focus on the drug substance elements of the program.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Productos Biológicos / Tecnología Farmacéutica / Industria Farmacéutica Idioma: En Revista: Biotechnol Bioeng Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Productos Biológicos / Tecnología Farmacéutica / Industria Farmacéutica Idioma: En Revista: Biotechnol Bioeng Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos