ISO/TR 22979:2017

Ophthalmic implants — Intraocular lenses — Guidance on assessment of the need for clinical investigation of intraocular lens design modifications

Ophthalmic implants — Intraocular lenses — Guidance on assessment of the need for clinical investigation of intraocular lens design modifications

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Referenced standards

IEC 62366-1:2015ISO 11979-10:2006ISO 11979-1:2012ISO 11979-2:2014ISO 11979-3:2012ISO 11979-4:2008ISO 11979-5:2006ISO 11979-6:2014ISO 11979-7:2014ISO 11979-8:2006ISO 11979-9:2006ISO 13485:2016ISO 14971:2007
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ISO/TR 22979:2017

Ophthalmic implants — Intraocular lenses — Guidance on assessment of the need for clinical investigation of intraocular lens design modifications

Ophthalmic implants — Intraocular lenses — Guidance on assessment of the need for clinical investigation of intraocular lens design modifications

ISO/TR 22979:2017 provides guidance on the application of all parts of the ISO 11979 series of International Standards for intraocular lenses (IOLs).[1?9] It addresses factors to be considered in the risk management process of modifications to anterior and posterior chamber IOLs in accordance with ISO 14971.[11] It also suggests methods of data analysis and interpretation that can be used to determine the need for a clinical investigation and its design.

Edition2017
Published Date2017
Published ByInternational Standardization Organisation/Technical Reference
Page Count22