ISO 20072:2009

Aerosol drug delivery device design verification — Requirements and test methods

Aerosol drug delivery device design verification — Requirements and test methods

Digital Document2009 edition2009Purchase Options

Referenced standards

IEC 60068-2-27IEC 60068-2-30:2005IEC 60068-2-32IEC 60068-2-64IEC 60601-1IEC 60601-1-2IEC 60721-3-7IEC 61000-4-2IEC 61000-4-3IEC 62304IEC 62366ISO 10993-1ISO 11135-1ISO 14971:2007ISO 15223-1ISO 17665-1
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Aerosol drug delivery device design verification — Requirements and test methods

ISO 20072:2009 applies to the design, labelling, instructions for use and testing requirements for hand-held single- and multi-use aerosol drug delivery devices (ADDDs) intended to deliver a metered or pre-metered aerosolized medication to or by means of the human respiratory tract (including nasal, oral, tracheal, bronchial and alveolar sites). This International Standard applies to both refillable and disposable devices intended for personal use.

ISO 20072:2009 is intended for device design verification and not for drug product quality assessment. The objective of this International Standard is to verify, by laboratory (in-vitro) testing, that the ADDD design consistently meets the manufacturer’s design specification by satisfying a device functionality profile and system verification test both of which are determined from a risk assessment and evaluated in accordance with the instructions for use.

Edition2009
Published Date2009
Published ByInternational Standardization Organisation
Page Count43