Regulatory Perspectives on Continuous Pharmaceutical Manufacturing: Moving From Theory to Practice-Reference-Cited by-同舟云学术

Regulatory Perspectives on Continuous Pharmaceutical Manufacturing: Moving From Theory to Practice

Published:2017-11 Issue:11 Volume:106 Page:3199-3206
ISSN:0022-3549
Container-title:Journal of Pharmaceutical Sciences
language:en
Short-container-title:Journal of Pharmaceutical Sciences

Author:

Nasr Moheb M.,Krumme Markus,Matsuda Yoshihiro,Trout Bernhardt L.,Badman Clive,Mascia Salvatore,Cooney Charles L.,Jensen Keith D.,Florence Alastair,Johnston Craig,Konstantinov Konstantin,Lee Sau L.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference16 articles.

1. Regulatory and quality considerations for continuous manufacturing. May 20-21, 2014 Continuous Manufacturing Symposium;Allison;J Pharm Sci,2015

2. Achieving continuous manufacturing for final dosage formation: challenges and how to meet them. May 20-21, 2014 Continuous Manufacturing Symposium;Byrn;J Pharm Sci,2015

3. White paper on continuous bioprocessing. May 20-21, 2014 Continuous Manufacturing Symposium;Konstantinov;J Pharm Sci,2015

4. Equipment and analytical companies meeting continuous challenges. May 20-21, 2014 Continuous Manufacturing Symposium;Page;J Pharm Sci,2015

5. Control systems engineering in continuous pharmaceutical manufacturing. May 20-21, 2014 Continuous Manufacturing Symposium;Myerson;J Pharm Sci,2014

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