EN ISO 11980:2012
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Ophthalmic optics - Contact lenses and contact lens care products - Guidance for clinical investigations (ISO 11980:2012)
15-11-2012
15-05-2013
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Clinical investigational requirements
Annex A (informative) - Elements of a clinical
investigation
Annex B (informative) - Procedures for the evaluation
of safety, physiological
performance and effect on
ocular tissues
Annex C (informative) - The evaluation of visual,
refractive and lens performance
and subject acceptance
Bibliography
ISO 11980:2012 gives guidelines for the clinical investigation of the safety and performance of contact lenses and contact lens care products.
| Committee |
CEN/TC 170
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Withdrawn
|
| Standards | Relationship |
| BS EN ISO 11980:2012 | Identical |
| SS-EN ISO 11980:2012 | Identical |
| NF EN ISO 11980 : 2013 | Identical |
| NBN EN ISO 11980 : 2013 | Identical |
| NS EN ISO 11980 : 2012 | Identical |
| NEN EN ISO 11980 : 2012 | Identical |
| I.S. EN ISO 11980:2012 | Identical |
| PN EN ISO 11980 : 2013 | Identical |
| ISO 11980:2012 | Identical |
| DS EN ISO 11980 : 2012 | Identical |
| UNE-EN ISO 11980:2013 | Identical |
| DIN EN ISO 11980:2013-03 | Identical |
| BS 7208-16(1998) : 1998 | Identical |
| ISO 18369-1:2017 | Ophthalmic optics — Contact lenses — Part 1: Vocabulary, classification system and recommendations for labelling specifications |
| ISO 14534:2011 | Ophthalmic optics — Contact lenses and contact lens care products — Fundamental requirements |
| ISO 13485:2016 | Medical devices — Quality management systems — Requirements for regulatory purposes |
| ISO 9001:2015 | Quality management systems — Requirements |
| ISO 14155:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice |
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