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Design of an Integrated Continuous Manufacturing System

By Oka, Sarang S; Escotet-Espinoza, M Sebastian Singh, Ravendra Scicolone, James V Hausner, Douglas B Ierapetritou, Marianthi; Muzzio, Fernando J

Published on

Abstract

This chapter presents a systematic, 12-step approach for designing, implementing, integrating, optimizing, and validating a continuous manufacturing system. Wherever appropriate, it also discusses the regulatory relevance of the technology integration effort. When considering the development of a continuous manufacturing facility, the industrial practitioner is well advised to consider very carefully not only the short-term intended use of the facility, but also other needs and demands that are likely to emerge. The implementation and efficient operation of an integrated continuous facility requires a heavy dose of "process engineering" skills. A thorough understanding of pharmaceutical raw materials and intermediate blends is crucial to the successful design of a robust continuous process, wherein achieving and maintaining a steady operation is paramount. Once the properties of individual materials have been examined, the next step in the design and development of a continuous process is the characterization of individual unit operations using the actual, characterized process materials.

Journal

Continuous Manufacturing of Pharmaceuticals. 2017, 405-446

DOI

10.1002/9781119001348.ch12

Type of publication

Chapter Book

Affiliations

  • Rutgers, The State University of New Jersey

Article Classification

Review article

Classification Areas

  • Oral doses
  • Modeling

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