NEN EN ISO 11979-7 : 2014
Withdrawn
Withdrawn
View Superseded by
OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 7: CLINICAL INVESTIGATIONS
Published date
01-12-2013
Publisher
Withdrawn date
10-31-2018
Superseded by
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Foreword
1 Scope
2 Normative references
3 Terms and definitions
4 Justification for a clinical investigation
5 Ethical considerations
6 General requirements
6.1 General
6.2 Additional requirements
Annex A (informative) Elements of a clinical investigation
Annex B (informative) Evaluation of post-operative adverse
event and visual acuity rates
Bibliography
Defines particular requirements for clinical investigations for posterior and anterior chamber intraocular lenses (IOLs).
| DevelopmentNote |
Supersedes NEN EN 13503-7. (06/2006)
|
| DocumentType |
Standard
|
| PublisherName |
Netherlands Standards
|
| Status |
Withdrawn
|
| SupersededBy |
| Standards | Relationship |
| NS EN ISO 11979-7 : 2014 | Identical |
| BS EN ISO 11979-7:2014 | Identical |
| DIN EN ISO 11979-7:2014-12 | Identical |
| EN ISO 11979-7:2018 | Identical |
| ISO 11979-7:2014 | Identical |
| I.S. EN ISO 11979-7:2014 | Identical |
| NBN EN ISO 11979-7 : 2014 | Identical |
| NF EN ISO 11979-7 : 2014 | Identical |
| UNE-EN ISO 11979-7:2015 | Identical |
Summarise
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