ISO 11040-8:2016

Prefilled syringes — Part 8: Requirements and test methods for finished prefilled syringes

Prefilled syringes — Part 8: Requirements and test methods for finished prefilled syringes

Digital Document2016 edition2016Purchase Options

Referenced standards

IEC 62366:2007IEC 80369-5:2016ISO 10993-1:2009ISO 11040-4:2015ISO 11040-5:2012ISO 11040-6:2012ISO 11608-1:2014ISO 11608-2:2012ISO 11608-3:2012ISO 11608-4:2006ISO 11608-5:2012ISO 13408-1:2008ISO 14971:2007ISO 17665-1:2006ISO 23908:2011ISO 7864:2016ISO 80369-1:2010ISO 80369-20:2015ISO 80369-3:2016ISO 80369-6:2016ISO 80369-7:2016ISO 9626:2016
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ISO 11040-8:2016

Prefilled syringes — Part 8: Requirements and test methods for finished prefilled syringes

Prefilled syringes — Part 8: Requirements and test methods for finished prefilled syringes

ISO 11040-8:2016 is applicable to aseptically filled or terminally sterilized finished prefilled syringes (intended for single use only) based on ISO 11040-4 or ISO 11040-6, together with ISO 11040-5, for parenteral injection preparations with focus on quality, functional performance and safety requirements, as well as relevant test methods.

Finished prefilled syringes which have undergone an additional preparation step by the user before injection (e.g. diluent syringes that have been emptied for reconstitution and in which the reconstituted drug solution has been aspirated after reconstitution) are excluded from the scope of ISO 11040-8:2016.

Edition2016
Standard Part No8
Published Date2016
Published ByInternational Standardization Organisation
Page Count9