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  1. #2513089

    I gcás inar lú an seilfré ná 2 bhliain, déanfar an seilfré a thuairisciú i míonna.

    Where shelf life is less than two years, the shelf life in months, shall be reported.

    Commission Regulation (EU) 2022/1440 of 31 August 2022 amending Regulation (EU) No 284/2013 as regards the information to be submitted for plant protection products and the specific data requirements for plant protection products containing micro-organisms (Text with EEA relevance)

  2. #2845588

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage Shelf-life:

    Commission Implementing Regulation (EU) 2023/1161 of 2 June 2023 granting a Union authorisation for the single biocidal product ‘Spray On’ in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)

  3. #1735717

    San áireamh sna conclúidí beidh torthaí na n-anailísí, mar údar leis an tseilfré mholta agus más iomchuí, an tseilfré atá in úsáid, faoi dhálaí molta stórála agus sonraíochtaí don táirge críochnaithe ag deireadh a sheilfré, agus seilfré in-úsáide más iomchuí, den táirge críochnaithe faoi na dálaí molta stórála sin.

    The conclusions shall contain the results of analyses, justifying the proposed shelf life and if appropriate, the in-use shelf life, under the recommended storage conditions and the specifications of the finished product at the end of the shelf life, and in-use shelf life if appropriate, of the finished product under these recommended storage conditions.

    Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)

  4. #342860

    ionadú ar shiúcraí i gcás ina gceadaíonn sé sin fad a chur le seilfré an bhia;

    replacing sugars where this permits an increase in the shelf-life of the food;

    Regulation (EC) No 1333/2008 of the European Parliament and of the Council of 16 December 2008 on food additives

  5. #516306

    (p) dálaí stórála agus seilfré an táirge bhithicídigh, faoi ghnáthdhálaí stórála;

    (p) conditions of storage and shelf-life of the biocidal product under normal conditions of storage;

    Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products Text with EEA relevance

  6. #517373

    3.4.Cobhsaíocht le linn stórála — cobhsaíocht agus seilfré

    3.4.Storage stability, stability and shelf-life

    Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products Text with EEA relevance

  7. #517404

    3.5.Cobhsaíocht le linn stórála — cobhsaíocht agus seilfré

    3.5.Storage stability, stability and shelf-life

    Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products Text with EEA relevance

  8. #743875

    cobhsaíocht, lena n-áirítear seilfré; agus

    stability, including shelf life; and

    Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. )

  9. #747459

    Tabharfar tuairisc sa Roinn seo ar staidéir maidir leis an maíomh seilfré, cobhsaíocht in úsáid agus cobhsaíocht muiriompair.

    This Section shall describe claimed shelf life, in use stability and shipping stability studies.

    Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance. )

  10. #747460

    An maíomh seilfré

    Claimed shelf-life

    Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance. )

  11. #747468

    na conclúidí agus an maíomh seilfré.

    the conclusions and claimed shelf life.

    Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance. )

  12. #1736182

    Déanfar sonraí mar thacaíocht leis an tseilfré mholta don táirge athbhunaithe a thíolacadh.

    Data in support of the proposed shelf life for the reconstituted product shall be submitted.

    Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)

  13. #1736184

    Beidh an tseilfré atá beartaithe inchosanta.

    The proposed in-use shelf life shall be justified.

    Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)

  14. #1911896

    Ní dhéanfar aon athrú ar na dálaí stórála, ar an tseilfré ná ar na sonraíochtaí.

    No change shall be made to the storage conditions, the shelf-life and the specifications.

    Commission Implementing Regulation (EU) 2021/17 of 8 January 2021 establishing a list of variations not requiring assessment in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  15. #1911995

    Ní bheidh athrú ar scaoileadh an táirge chríochnaithigh ná ar shonraíochtaí seilfré cé is moite den chuma.

    The finished product release and shelf life specifications shall not have been changed except for appearance.

    Commission Implementing Regulation (EU) 2021/17 of 8 January 2021 establishing a list of variations not requiring assessment in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  16. #1912001

    Ní bheidh athrú ar shonraíochtaí scaoilte ná ar shonraíochtaí seilfré an táirge.

    The release and end of shelf-life specifications of the product shall not have been changed.

    Commission Implementing Regulation (EU) 2021/17 of 8 January 2021 establishing a list of variations not requiring assessment in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  17. #1912065

    Fanfaidh an támhán, scaoileadh an táirge chríochnaithe agus na sonraíochtaí deireadh seilfré mar an gcéanna.

    The excipient, finished product release and end of shelf life specifications shall remain the same.

    Commission Implementing Regulation (EU) 2021/17 of 8 January 2021 establishing a list of variations not requiring assessment in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  18. #1912106

    Athrú ar sheilfré nó ar phrótacal cobhsaíochta formheasta an táirge chríochnaithe:

    Change in the shelf-life or to an approved stability protocol of the finished product:

    Commission Implementing Regulation (EU) 2021/17 of 8 January 2021 establishing a list of variations not requiring assessment in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  19. #1912119

    Fanfaidh scaoileadh an táirge chríochnaithe agus sonraíochtaí deireadh seilfré mar an gcéanna.

    The finished product release and end of shelf life specifications shall remain the same.

    Commission Implementing Regulation (EU) 2021/17 of 8 January 2021 establishing a list of variations not requiring assessment in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  20. #1933538

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2021/368 of 1 March 2021 granting a Union authorisation for the single biocidal product ‘Aero-Sense Aircraft Insecticide ASD’ (Text with EEA relevance)

  21. #1933542

    Seilfré: 2 bhliain

    Shelf life: 2 years

    Commission Implementing Regulation (EU) 2021/368 of 1 March 2021 granting a Union authorisation for the single biocidal product ‘Aero-Sense Aircraft Insecticide ASD’ (Text with EEA relevance)

  22. #2011317

    Coinníollacha stórála agus seilfré an táirge faoi ghnáthchoinníollacha stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2021/552 of 30 March 2021 granting a Union authorisation for the biocidal product family ‘DEC-AHOL® Product Family’ (Text with EEA relevance)

  23. #2011322

    Seilfré: 2 bhliain

    Shelf-life: 2 years

    Commission Implementing Regulation (EU) 2021/552 of 30 March 2021 granting a Union authorisation for the biocidal product family ‘DEC-AHOL® Product Family’ (Text with EEA relevance)

  24. #2049702

    Áireofar sna conclúidí torthaí na n-anailísí, lena dtugtar údar leis an tseilfré a bheartaítear agus, más iomchuí, leis an tseilfré in úsáid, faoi na dálaí stórála a mholtar.

    The conclusions shall contain the results of analyses, justifying the proposed shelf life and if appropriate, the in-use shelf life, under the recommended storage conditions.

    Commission Delegated Regulation (EU) 2021/805 of 8 March 2021 amending Annex II to Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  25. #2050064

    Tabharfar tuairisc ar na tástálacha a dhéantar chun tacú leis an tseilfré, na dálaí molta stórála agus na sonraíochtaí ag deireadh na seilfré a mholann an t-iarratasóir.

    A description shall be given of the tests undertaken to support the shelf life, the recommended storage conditions and the specifications at the end of the shelf life proposed by the applicant.

    Commission Delegated Regulation (EU) 2021/805 of 8 March 2021 amending Annex II to Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  26. #2050070

    Déanfar sonraí a chur isteach mar thacaíocht leis an tseilfré mholta don táirge athbhunaithe a cuireadh isteach.

    Data in support of the proposed shelf life for the reconstituted product shall be submitted.

    Commission Delegated Regulation (EU) 2021/805 of 8 March 2021 amending Annex II to Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  27. #2077256

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2021/977 of 7 June 2021 amending Implementing Regulation (EU) 2019/1844 to make administrative changes to the Union authorisation of the biocidal product family ‘BPF_Iodine_VET’ (Text with EEA relevance)

  28. #2077260

    Beatha ar sheilf: 12 mhí i HDPE

    Shelf-life: 12 months in HDPE

    Commission Implementing Regulation (EU) 2021/977 of 7 June 2021 amending Implementing Regulation (EU) 2019/1844 to make administrative changes to the Union authorisation of the biocidal product family ‘BPF_Iodine_VET’ (Text with EEA relevance)

  29. #2077409

    Beatha ar sheilf: 24 mhí i HDPE

    Shelf-life: 24 months in HDPE

    Commission Implementing Regulation (EU) 2021/977 of 7 June 2021 amending Implementing Regulation (EU) 2019/1844 to make administrative changes to the Union authorisation of the biocidal product family ‘BPF_Iodine_VET’ (Text with EEA relevance)

  30. #2077670

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2021/978 of 10 June 2021 granting a Union authorisation for the biocidal product family “Lyso IPA Surface Disinfection” (Text with EEA relevance)

  31. #2077671

    Seilfré: 36 mhí

    Shelf-life: 36 months

    Commission Implementing Regulation (EU) 2021/978 of 10 June 2021 granting a Union authorisation for the biocidal product family “Lyso IPA Surface Disinfection” (Text with EEA relevance)

  32. #2077706

    Seilfré: 24 mhí

    Shelf-life: 24 months

    Commission Implementing Regulation (EU) 2021/978 of 10 June 2021 granting a Union authorisation for the biocidal product family “Lyso IPA Surface Disinfection” (Text with EEA relevance)

  33. #2081359

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2021/1044 of 22 June 2021 granting a Union authorisation for the single biocidal product ‘Pesguard® Gel’ (Text with EEA relevance)

  34. #2081362

    Seilfré: 2 bhliain.

    Shelf life: 2 years.

    Commission Implementing Regulation (EU) 2021/1044 of 22 June 2021 granting a Union authorisation for the single biocidal product ‘Pesguard® Gel’ (Text with EEA relevance)

  35. #2082229

    ag a bhfuil seilfré nach lú ná 20 bliain, agus é sin arna dhearbhú ag an monaróir,

    with a shelf life declared by the manufacturer of not less than 20 years,

    Council Regulation (EU) 2021/1052 of 18 June 2021 amending Regulation (EU) No 1387/2013 suspending the autonomous Common Customs Tariff duties on certain agricultural and industrial products

  36. #2116294

    go bhfuil an chuid den seilfré nach bhfuil caite inghlactha;

    the remaining shelf life is acceptable;

    Commission Implementing Regulation (EU) 2021/1280 of 2 August 2021 as regards measures on good distribution practice for active substances used as starting materials in veterinary medicinal products in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  37. #2118413

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2021/1322 of 3 August 2021 amending Implementing Regulation (EU) 2019/2076 to make administrative changes to the Union authorisation of the biocidal product family ‘Contec IPA Product Family’ (Text with EEA relevance)

  38. #2118417

    Saol na seilfré: 2 bhliain

    Shelf-life: 2 years

    Commission Implementing Regulation (EU) 2021/1322 of 3 August 2021 amending Implementing Regulation (EU) 2019/2076 to make administrative changes to the Union authorisation of the biocidal product family ‘Contec IPA Product Family’ (Text with EEA relevance)

  39. #2187142

    ag a bhfuil seilfré nach lú ná 20 bliain, agus é sin arna dhearbhú ag an monaróir,

    with a shelf life declared by the manufacturer of not less than 20 years,

    Council Regulation (EU) 2021/2278 of 20 December 2021 suspending the Common Customs Tariff duties referred to in Article 56(2), point (c), of Regulation (EU) No 952/2013 on certain agricultural and industrial products, and repealing Regulation (EU) No 1387/2013

  40. #2290638

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2022/114 of 26 January 2022 granting a Union authorisation for the single biocidal product ‘SchwabEX-Guard’ (Text with EEA relevance)

  41. #2290641

    Seilfré: 2 bhliain.

    Shelf life: 2 years.

    Commission Implementing Regulation (EU) 2022/114 of 26 January 2022 granting a Union authorisation for the single biocidal product ‘SchwabEX-Guard’ (Text with EEA relevance)

  42. #2343723

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2022/527 of 1 April 2022 granting a Union authorisation for the single biocidal product ‘ARIEL chlorine Professional System 5 chlorine bleach for white wash’ (Text with EEA relevance)

  43. #2343737

    Seilfré: 12 mhí

    Shelf life: 12 months

    Commission Implementing Regulation (EU) 2022/527 of 1 April 2022 granting a Union authorisation for the single biocidal product ‘ARIEL chlorine Professional System 5 chlorine bleach for white wash’ (Text with EEA relevance)

  44. #2463434

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2022/964 of 10 June 2022 granting a Union authorisation for the biocidal product family ‘SOPUROXID’ (Text with EEA relevance)

  45. #2463436

    Is é 6 mhí an seilfré do gach táirge.

    The shelf life of the biocidal product is 6 months.

    Commission Implementing Regulation (EU) 2022/964 of 10 June 2022 granting a Union authorisation for the biocidal product family ‘SOPUROXID’ (Text with EEA relevance)

  46. #2475190

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2022/1185 of 8 July 2022 granting a Union authorisation for the biocidal product family ‘Contec Hydrogen Peroxide Biocidal Product Family’ (Text with EEA relevance)

  47. #2475196

    Seilfré: 24 mhí

    The shelf-life: 24 months.

    Commission Implementing Regulation (EU) 2022/1185 of 8 July 2022 granting a Union authorisation for the biocidal product family ‘Contec Hydrogen Peroxide Biocidal Product Family’ (Text with EEA relevance)

  48. #2475392

    Coinníollacha stórála agus seilfré an táirge de réir na ngnáthdhálaí stórála

    Conditions of storage and shelf-life of the product under normal conditions of storage

    Commission Implementing Regulation (EU) 2022/1186 of 8 July 2022 granting a Union authorisation for the biocidal product family ‘L+R Propanol PT1 Family’ (Text with EEA relevance)

  49. #2475394

    Seilfré: 36 mhí

    Shelf-life: 36 months

    Commission Implementing Regulation (EU) 2022/1186 of 8 July 2022 granting a Union authorisation for the biocidal product family ‘L+R Propanol PT1 Family’ (Text with EEA relevance)

  50. #2479316

    Seilfré 18 mí.

    Shelf life 18 months.

    Commission Implementing Regulation (EU) 2022/1226 of 14 July 2022 granting a Union authorisation for the single biocidal product ‘Bioquell HPV-AQ’ (Text with EEA relevance)