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prSSH EN ISO 11980:2025

Optikat oftalmike - Lentet e kontaktit dhe produktet e kujdesit për lentet e kontaktit - Udhëzues për investigimet klinike (ISO 11980:2025)

Ophthalmic optics - Contact lenses and contact lens care products - Requirements and guidance for clinical investigations (ISO 11980:2025)

General information

40.20     9 shk 2026

40.60    11 maj 2026

DPS

DPS/KT 316

European Norm

11.040.70  

Scope

This document gives requirements and guidelines for the clinical investigation (CI) to establish the safety and performance of contact lenses and contact lens care products.
NOTE 1        This document attempts to align the recognised regulatory requirements for the conduct of a CI to meet the marketing and labelling requirements for contact lenses and contact lens care products around the world. However, national requirements vary greatly. Wherever national practice or regulations dictate some legal requirement, this requirement takes precedence over this document.
NOTE 2        For indications beyond correction of refractive error, additional considerations for safety and performance are to be included in the clinical investigation plan (CIP).

Life cycle

PREVIOUSLY

PUBLISHED
SSH EN ISO 11980:2012

NOW

IN_DEVELOPMENT
prSSH EN ISO 11980:2025
40.20 DIS ballot initiated: 12 weeks
9 shk 2026

Related project

Adopted from EN ISO 11980:2025 IDENTICAL

Adopted from ISO 11980:2025 IDENTICAL

Preview

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