Literature DB >> 25830179

Regulatory and quality considerations for continuous manufacturing. May 20-21, 2014 Continuous Manufacturing Symposium.

Gretchen Allison, Yanxi Tan Cain, Charles Cooney, Tom Garcia, Tara Gooen Bizjak, Oyvind Holte, Nirdosh Jagota, Bekki Komas, Evdokia Korakianiti, Dora Kourti, Rapti Madurawe, Elaine Morefield, Frank Montgomery, Moheb Nasr, William Randolph, Jean-Louis Robert, Dave Rudd, Diane Zezza.   

Abstract

This paper assesses the current regulatory environment, relevant regulations and guidelines, and their impact on continuous manufacturing. It summarizes current regulatory experience and learning from both review and inspection perspectives. It outlines key regulatory aspects, including continuous manufacturing process description and control strategy in regulatory files, process validation, and key Good Manufacturing Practice (GMP) requirements. In addition, the paper identifies regulatory gaps and challenges and proposes a way forward to facilitate implementation.
© 2014 Wiley Periodicals, Inc. and the American Pharmacists Association.

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Year:  2015        PMID: 25830179

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  3 in total

1.  Continuous Manufacturing of Ketoprofen Delayed Release Pellets Using Melt Extrusion Technology: Application of QbD Design Space, Inline Near Infrared, and Inline Pellet Size Analysis.

Authors:  Anh Q Vo; Gerd Kutz; Herman He; Sagar Narala; Suresh Bandari; Michael A Repka
Journal:  J Pharm Sci       Date:  2020-09-08       Impact factor: 3.534

Review 2.  The Future of Pharmaceutical Manufacturing Sciences.

Authors:  Jukka Rantanen; Johannes Khinast
Journal:  J Pharm Sci       Date:  2015-08-17       Impact factor: 3.534

3.  Predictive Model-Based Process Start-Up in Pharmaceutical Continuous Granulation and Drying.

Authors:  Victoria Pauli; Peter Kleinebudde; Markus Krumme
Journal:  Pharmaceutics       Date:  2020-01-15       Impact factor: 6.321

  3 in total

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