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FDA/M-CERSI Co-Processed API Workshop Proceedings

delete2023-08-01
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PRE
AI
L
Luke Schenck *
P
Paresma Patel
R
Ramesh Sood *
L
Llorente Boñaga
P
Peter Capella
O
Olivier Dirat
D
Deniz Erdemir
S
Steven Ferguson
C
Cinzia Gazziola
L
Lindsey Saunders Gorka
L
Laurie Graham
S
Stephen W. Hoag
E
Ephrem Hunde
B
Billie J. Kline
S
Sau Larry Lee
R
Rapti D. Madurawe
I
Ivan Marziano
J
Jeremy M. Merritt
S
Sharon Page
J
James E. Polli
M
Mahesh Ramanadham
M
Mohan K. Sapru
B
Ben Stevens
T
Tim Watson
张海涛 (Haitao Zhang)
DOI:10.1016/j.xphs.2023.01.006delete
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Abstract

Abstract

En 中文
These proceedings contain presentation summaries and discussion highlights from the University of Mary-land Center of Excellence in Regulatory Science and Innovation (M-CERSI) Workshop on Co-processed API, held on July 13 and 14, 2022. This workshop examined recent advances in the use of co-processed active pharmaceutical ingredients as a technology to improve drug substance physicochemical properties and drug product manufacturing process robustness, and explored proposals for enabling commercialization of these transformative technologies. Regulatory considerations were discussed with a focus on the classification, CMC strategies, and CMC documentation supporting the use of this class of materials from clinical studies through commercialization. The workshop format was split between presentations from industry, academia and the FDA, followed by breakout sessions structured to facilitate discussion. Given co-processed API is a relatively new concept, the authors felt it prudent to compile these proceedings to gain further visibility to topics discussed and perspectives raised during the workshop, particularly during breakout discussions. Disclaimer: This paper reflects discussions that occurred among stakeholder groups, including FDA, on vari-ous topics. The topics covered in the paper, including recommendations, therefore, are intended to capture key discussion points. The paper should not be interpreted to reflect alignment on the different topics by the participants, and the recommendations provided should not be used in lieu of FDA published guidance or direct conversations with the Agency about a specific development program. This paper should not be con-strued to represent FDA's views or policies.& COPY; 2023 American Pharmacists Association. Published by Elsevier Inc. All rights reserved.
Keywords:
Co-processing
Co-processed API
Regulatory
Particle engineering

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Journal of Pharmaceutical Sciences cover
Journal of Pharmaceutical Sciences
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