Workshop on devices: regional issues surrounding regulatory requirements for nebulizers

David Alexander Vodden Morton; David Jefferys; J Ziegler; Pieter Zanen

Workshop on devices: regional issues surrounding regulatory requirements for nebulizers

David Alexander Vodden Morton, David Jefferys, J Ziegler, Pieter Zanen

Drug Delivery Disposition & Dynamics

Research output: Chapter in Book/Report/Conference proceeding › Conference Paper › Research › peer-review

Abstract

The nebulizer-drug-patient interface has arguably been a neglected area of regulation that has recently been the focus of efforts to harmonize standards and development guidelines at a global level. Further improvements in the quality of these standards and guidelines, as well as consistency of implementation, will need the input of all relevant stakeholders from the regulatory authorities, device and drug industries as well as academicians and practitioners with clinical and pharmaceutical expertise. This workshop is intended to stimulate the debate and our understanding of the major issues surrounding nebulizer development and regulation in a global marketplace.

Original language	English
Title of host publication	Respiratory Drug Delivery 2009
Editors	P R Bryon, J Peart, J D Suman, P M Young
Place of Publication	USA
Publisher	Davis Healthcare International Publishing
Pages	129 - 139
Number of pages	11
Volume	1
ISBN (Print)	1933722304
Publication status	Published - 2009
Event	Respiratory Drug Delivery 2009 - Lisbon, Portugal, USA Duration: 1 Jan 2009 → …

Conference

Conference	Respiratory Drug Delivery 2009
City	USA
Period	1/01/09 → …

Cite this

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title = "Workshop on devices: regional issues surrounding regulatory requirements for nebulizers",

abstract = "The nebulizer-drug-patient interface has arguably been a neglected area of regulation that has recently been the focus of efforts to harmonize standards and development guidelines at a global level. Further improvements in the quality of these standards and guidelines, as well as consistency of implementation, will need the input of all relevant stakeholders from the regulatory authorities, device and drug industries as well as academicians and practitioners with clinical and pharmaceutical expertise. This workshop is intended to stimulate the debate and our understanding of the major issues surrounding nebulizer development and regulation in a global marketplace.",

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booktitle = "Respiratory Drug Delivery 2009",

publisher = "Davis Healthcare International Publishing",

note = "Respiratory Drug Delivery 2009 ; Conference date: 01-01-2009",

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Workshop on devices: regional issues surrounding regulatory requirements for nebulizers. / Morton, David Alexander Vodden; Jefferys, David; Ziegler, J et al.
Respiratory Drug Delivery 2009. ed. / P R Bryon; J Peart; J D Suman; P M Young. Vol. 1 USA: Davis Healthcare International Publishing, 2009. p. 129 - 139.

Research output: Chapter in Book/Report/Conference proceeding › Conference Paper › Research › peer-review

TY - GEN

T1 - Workshop on devices: regional issues surrounding regulatory requirements for nebulizers

AU - Morton, David Alexander Vodden

AU - Jefferys, David

AU - Ziegler, J

AU - Zanen, Pieter

PY - 2009

Y1 - 2009

N2 - The nebulizer-drug-patient interface has arguably been a neglected area of regulation that has recently been the focus of efforts to harmonize standards and development guidelines at a global level. Further improvements in the quality of these standards and guidelines, as well as consistency of implementation, will need the input of all relevant stakeholders from the regulatory authorities, device and drug industries as well as academicians and practitioners with clinical and pharmaceutical expertise. This workshop is intended to stimulate the debate and our understanding of the major issues surrounding nebulizer development and regulation in a global marketplace.

AB - The nebulizer-drug-patient interface has arguably been a neglected area of regulation that has recently been the focus of efforts to harmonize standards and development guidelines at a global level. Further improvements in the quality of these standards and guidelines, as well as consistency of implementation, will need the input of all relevant stakeholders from the regulatory authorities, device and drug industries as well as academicians and practitioners with clinical and pharmaceutical expertise. This workshop is intended to stimulate the debate and our understanding of the major issues surrounding nebulizer development and regulation in a global marketplace.

M3 - Conference Paper

SN - 1933722304

VL - 1

SP - 129

EP - 139

BT - Respiratory Drug Delivery 2009

A2 - Bryon, P R

A2 - Peart, J

A2 - Suman, J D

A2 - Young, P M

PB - Davis Healthcare International Publishing

CY - USA

T2 - Respiratory Drug Delivery 2009

Y2 - 1 January 2009

ER -