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Continuous freeze-drying and its relevance to the pharma/biotech industry

Research output: Contribution to conference - Without ISBN/ISSN Abstractpeer-review

Published

Standard

Continuous freeze-drying and its relevance to the pharma/biotech industry. / Pisano, Roberto; Capozzi, Luigi; Trout, Bernhardt L.
2017. Abstract from Integrated Continuous Biomanufacturing III, Cascais, Portugal.

Research output: Contribution to conference - Without ISBN/ISSN Abstractpeer-review

Harvard

Pisano, R, Capozzi, L & Trout, BL 2017, 'Continuous freeze-drying and its relevance to the pharma/biotech industry', Integrated Continuous Biomanufacturing III, Cascais, Portugal, 17/09/17 - 21/09/17.

APA

Pisano, R., Capozzi, L., & Trout, B. L. (2017). Continuous freeze-drying and its relevance to the pharma/biotech industry. Abstract from Integrated Continuous Biomanufacturing III, Cascais, Portugal.

Vancouver

Pisano R, Capozzi L, Trout BL. Continuous freeze-drying and its relevance to the pharma/biotech industry. 2017. Abstract from Integrated Continuous Biomanufacturing III, Cascais, Portugal.

Author

Pisano, Roberto ; Capozzi, Luigi ; Trout, Bernhardt L. / Continuous freeze-drying and its relevance to the pharma/biotech industry. Abstract from Integrated Continuous Biomanufacturing III, Cascais, Portugal.

Bibtex

@conference{e83c333786fc4ba79213bb399ba4768d,
title = "Continuous freeze-drying and its relevance to the pharma/biotech industry",
abstract = "The new paradigm of pharmaceutical industry is to move from batch to continuous processes in order to satisfy the stringent requirements of quality, safety and efficiency set by regulatory authorities and reduce production costs. In this perspective, freeze-drying needs to be completely rethought in order to be more integrated in the chain of production of drugs, more flexible to respond to variations in market needs and allowing the monitoring of product quality. The future of freeze-drying, as a downstream process, is therefore to move from batch to continuous. Over the past decades many ideas regarding continuous freeze-drying has been proposed, but none of them has been successfully applied. The objective of this work is to demonstrate the feasibility of an innovative concept to produce lyophilized unit-dose drugs using a continuous process. This novel strategy was demonstrated to improve both yield and vial-to-vial uniformity, giving all those advantages that are typical of continuous technology such as flexibility and elimination of process scale-up from laboratory to industrial scale. ",
author = "Roberto Pisano and Luigi Capozzi and Trout, {Bernhardt L.}",
year = "2017",
language = "English",
note = "Integrated Continuous Biomanufacturing III ; Conference date: 17-09-2017 Through 21-09-2017",

}

RIS

TY - CONF

T1 - Continuous freeze-drying and its relevance to the pharma/biotech industry

AU - Pisano, Roberto

AU - Capozzi, Luigi

AU - Trout, Bernhardt L.

PY - 2017

Y1 - 2017

N2 - The new paradigm of pharmaceutical industry is to move from batch to continuous processes in order to satisfy the stringent requirements of quality, safety and efficiency set by regulatory authorities and reduce production costs. In this perspective, freeze-drying needs to be completely rethought in order to be more integrated in the chain of production of drugs, more flexible to respond to variations in market needs and allowing the monitoring of product quality. The future of freeze-drying, as a downstream process, is therefore to move from batch to continuous. Over the past decades many ideas regarding continuous freeze-drying has been proposed, but none of them has been successfully applied. The objective of this work is to demonstrate the feasibility of an innovative concept to produce lyophilized unit-dose drugs using a continuous process. This novel strategy was demonstrated to improve both yield and vial-to-vial uniformity, giving all those advantages that are typical of continuous technology such as flexibility and elimination of process scale-up from laboratory to industrial scale.

AB - The new paradigm of pharmaceutical industry is to move from batch to continuous processes in order to satisfy the stringent requirements of quality, safety and efficiency set by regulatory authorities and reduce production costs. In this perspective, freeze-drying needs to be completely rethought in order to be more integrated in the chain of production of drugs, more flexible to respond to variations in market needs and allowing the monitoring of product quality. The future of freeze-drying, as a downstream process, is therefore to move from batch to continuous. Over the past decades many ideas regarding continuous freeze-drying has been proposed, but none of them has been successfully applied. The objective of this work is to demonstrate the feasibility of an innovative concept to produce lyophilized unit-dose drugs using a continuous process. This novel strategy was demonstrated to improve both yield and vial-to-vial uniformity, giving all those advantages that are typical of continuous technology such as flexibility and elimination of process scale-up from laboratory to industrial scale.

M3 - Abstract

T2 - Integrated Continuous Biomanufacturing III

Y2 - 17 September 2017 through 21 September 2017

ER -