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Section VI – Recording of identity checks
Part C of Section I must be used to record modifications to identification details.
Section VI – Recording of identity checks
Part C of Section I must be used to record modifications to identification details.
Seirbhís um Bainistiú Aitheantais agus Rochtana (Identity and Access Management Service, IAM)
Identity and Access Management Service (IAM)
(j) as to the identity of the supplier or distributor, or the standing, commercial importance, competence or capabilities of, the manufacturer, producer, supplier or distributor, of any goods, or
( j ) as to the identity of the supplier or distributor, or the standing, commercial importance, competence or capabilities of, the manufacturer, producer, supplier or distributor, of any goods, or
Furthermore, the Irish nation cherishes its special affinity with people of Irish ancestry living abroad who share its cultural identity and heritage.
Furthermore, the Irish nation cherishes its special affinity with people of Irish ancestry living abroad who share its cultural identity and heritage.
Furthermore, the Irish nation cherishes its special affinity with people of Irish ancestry living abroad who share its cultural identity and heritage.
Furthermore, the Irish nation cherishes its special affinity with people of Irish ancestry living abroad who share its cultural identity and heritage.
Méthode alternative de vérification d’identité (si applicable)/Alternative method for identity verification (if applicable)/Modh malartach fíorúcháin sainaitheantais (más infheidhme)
Méthode alternative de vérification d’identité (si applicable)/Alternative method for identity verification (if applicable)/official language:
Nom (en lettres capitales), qualité de la personne ayant vérifié 1’identité et signature Name (in capital letters), capacity of official verifying the identity and signature,
Nom (en lettres capitales), qualité de la personne ayant vérifié 1’identité et signature
Thug an Coimisiún chun suntais sa teachtaireacht uaidh an 14 Samhain 2017 dar teideal “Strengthening European identity through education and culture” [An Fhéiniúlacht Eorpach a neartú trí Oideachas agus Cultúr], ról lárnach atá ag an oideachas, an cultúr agus an spórt chun saoránacht ghníomhach agus luachanna comhchoiteanna a chur chun cinn i measc na nglún is óige.
In its communication of 14 November 2017 entitled ‘Strengthening European identity through education and culture’, the Commission highlighted the pivotal role that education, culture and sport play in promoting active citizenship and common values among the youngest generations.
Whenever laws and regulations so require, checks conducted on the identity of the equine animal must be recorded by the competent authority, the delegated body or by the organisation which manages registered horses for competitions or races.
Section II – Administration of medicinal products
Information sur toute autre méthode appropriée donnant des garanties pour vérifier l’identité de l’animal (groupe sanguin/code ADN) (optionnel)/Information on any other appropriate method providing guarantees to verify the identity of the animal (blood group/DNA code) (optional)/Faisnéis maidir le haon mhodh eile iomchuí lena soláthraítear ráthaíochtaí chun sainaitheantas an ainmhí a fhíorú (grúpa fola/cód DNA) (roghnach)
Information sur toute autre méthode appropriée donnant des garanties pour vérifier l’identité de l’animal (groupe sanguin/code ADN) (optionnel)/Information on any other appropriate method providing guarantees to verify the identity of the animal (blood group/DNA code) (optional)/official language:
L’identité de l’équidé doit être contrôlée chaque fois que les lois et règlements 1’exigent et il doit être certifié qu’elle est conforme à la description donnée dans la section I du document d’identification. The identity of the equine animal must be checked each time this is required by the rules and regulations and certified that it conforms to the description given in Section I of the identification document.
L’identité de l’équidé doit être contrôlée chaque fois que les lois et règlements 1’exigent et il doit être certifié qu’elle est conforme à la description donnée dans la section I du document d’identification.
Sa tástáil um chobhsaíocht stórála comhthimpeallaí fadtéarmaí, tabharfar aghaidh ar airíonna ábhartha fisiceacha, ceimiceacha agus teicniúla an táirge sin idir roimh an stóráil agus ina diaidh, i gcomhréir le roinn 2.6.4 de Guidance on the Biocidal Products Regulation Volume I: Identity of the active substance/physico-chemical properties/analytical methodology – Information Requirements, Evaluation and Assessment (ECHA, March 2022) [Treoraíocht maidir le Rialachán na dTáirgí Bithicídeacha Imleabhar I: Aitheantas na substainte gníomhaí/na n-airíonna fisiciceimiceacha/na modheolaíochta anailísí (ECHA, Márta 2022)], chun seilfré 24 mhí a dheimhniú.
The long-term ambient storage stability test shall address the relevant physical, chemical and technical properties of that product both prior to and after storage in accordance with section 2.6.4 of the Guidance on the Biocidal Products Regulation Volume I: Identity of the active substance/physico-chemical properties/analytical methodology – Information Requirements, Evaluation and Assessment (ECHA, March 2022), in order to confirm a shelf life of 24 months.
Sa tástáil um chobhsaíocht stórála comhthimpeallaí fadtéarmaí, tabharfar aghaidh ar airíonna ábhartha fisiceacha, ceimiceacha agus teicniúla na dtáirgí sin idir roimh an stóráil agus ina diaidh, i gcomhréir le roinn 2.6.4 de Guidance on the Biocidal Products Regulation Volume I: Identity of the active substance/physico-chemical properties/analytical methodology – Information Requirements, Evaluation and Assessment (ECHA, March 2022) [Treoraíocht maidir le Rialachán na dTáirgí Bithicídeacha Imleabhar I: Aitheantas na substainte gníomhaí/na n-airíonna fisiciceimiceacha/na modheolaíochta anailísí (ECHA, Márta 2022)], chun seilfré 24 mhí a dheimhniú.
The long-term ambient storage stability test shall address the relevant physical, chemical and technical properties of the products both prior to and after storage in accordance with section 2.6.4 of the Guidance on the Biocidal Products Regulation Volume I: Identity of the active substance/physico-chemical properties/analytical methodology – Information Requirements, Evaluation and Assessment (ECHA, March 2022), in order to confirm a shelf life of 24 months.