BS EN ISO 11979-7:2014
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Ophthalmic implants. Intraocular lenses Clinical investigations
Hardcopy , PDF
05-06-2018
English
30-09-2014
Foreword
1 Scope
2 Normative references
3 Terms and definitions
4 Justification for a clinical investigation
5 Ethical considerations
6 General requirements
Annex A (informative) - Elements of a clinical
investigation
Annex B (informative) - Evaluation of post-operative
adverse event and visual acuity rates
Annex C (informative) - Additional elements for toric
IOLs
Annex D (informative) - Additional elements for
accommodating IOLs
Annex E (informative) - Clinical tests
Bibliography
Defines particular requirements for clinical investigations for posterior and anterior chamber intraocular lenses (IOLs).
Committee |
CH/172/7
|
DevelopmentNote |
Supersedes BS EN 13503-7 and 04/30103843 DC. (05/2006) Supersedes 12/30218032 DC. (09/2014)
|
DocumentType |
Standard
|
Pages |
50
|
PublisherName |
British Standards Institution
|
Status |
Superseded
|
SupersededBy | |
Supersedes |
Standards | Relationship |
UNI EN ISO 11979-7 : 2015 | Identical |
NBN EN ISO 11979-7 : 2014 | Identical |
SN EN ISO 11979-7 : 2014 | Identical |
NF EN ISO 11979-7 : 2014 | Identical |
ONORM EN ISO 11979-7 : 2015 | Identical |
NS EN ISO 11979-7 : 2014 | Identical |
NEN EN ISO 11979-7 : 2014 | Identical |
DIN EN ISO 11979-7:2014-12 | Identical |
ISO 11979-7:2014 | Identical |
I.S. EN ISO 11979-7:2014 | Identical |
UNE-EN ISO 11979-7:2015 | Identical |
EN ISO 11979-7:2014 | Identical |
EN ISO 11979-7:2018 | Identical |
ISO 11979-10:2006 | Ophthalmic implants Intraocular lenses Part 10: Phakic intraocular lenses |
ISO/TR 22979:2017 | Ophthalmic implants — Intraocular lenses — Guidance on assessment of the need for clinical investigation of intraocular lens design modifications |
ISO 11979-1:2006 | Ophthalmic implants Intraocular lenses Part 1: Vocabulary |
ISO 14155:2011 | Clinical investigation of medical devices for human subjects Good clinical practice |
ISO 14971:2007 | Medical devices Application of risk management to medical devices |
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