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77 results in 14 documents

  1. #1736116

    Beidh na tástálacha agus na rialuithe a dhéanfar oiriúnach don ábhar tosaigh.

    The tests and controls conducted shall be appropriate to the starting material.

    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)

  2. #1736140

    feidhm an ábhair thosaigh,

    the function of the starting material,

    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)

  3. #1911833

    ábhar tosaigh;

    a starting material;

    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)

  4. #1911838

    le haghaidh na substainte gníomhaí nó ábhar tosaigh, nó imoibrí nó idirmheánach den chuid na substainte gníomhaí;

    for the active substance or a starting material, reagent or intermediate of the active substance;

    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)

  5. #1911871

    le haghaidh ábhar tosaigh, imoibrí nó idirmheánaigh a úsáidtear i modh monaraíochta na substainte gníomhaí;

    for a starting material, reagent or intermediate used in the manufacturing process of the active substance;

    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)

  6. #1911872

    le haghaidh ábhar tosaigh, nó imoibrí nó idirmheánach de shubstaint gníomhach;

    for a starting material, reagent or intermediate of an active substance;

    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)

  7. #1911903

    Athrú chuig prótacal cobhsaíochta formheasta substainte gníomhaí (lena n-áirítear ábhar tosaigh, imoibrí nó idirmheánach)

    Change to an approved stability protocol of an active substance (including starting material, reagent or intermediate)

    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)

  8. #1912117

    ábhar tosaigh, imoibrí nó idirmheánach a úsáidtear i modh monaraíochta na substainte gníomhaí;

    starting material, reagent or intermediate used in the manufacturing process of the active substance;

    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)

  9. #1912127

    ábhar tosaigh, imoibrí, idirmheánach a úsáidtear i modh monaraíochta na substainte gníomhaí;

    starting material, reagent, intermediate used in the manufacturing process of the active substance;

    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)

  10. #2049370

    Táirgeadh ábhair tosaigh agus rialú air

    Production and control of starting material

    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)

  11. #2049984

    Maidir le meáin saothrúcháin a úsáidtear chun na substaintí gníomhacha a tháirgeadh, measfar gur ábhar tosaigh amháin iad.

    Culture media used for production of the active substances shall be regarded as one starting material.

    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)

  12. #2050017

    feidhm an ábhair tosaigh;

    the function of the starting material;

    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)

  13. #2116302

    ainm nó ainmniú na substainte gníomhaí a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta;

    name or designation of the active substance used as a starting material in veterinary medicinal products;

    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)

  14. #2116303

    baiscuimhir na substainte gníomhaí a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta;

    batch number of the active substance used as a starting material in veterinary medicinal products;

    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)

  15. #2116304

    cainníocht na substainte gníomhaí a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta a cuireadh ar ais;

    quantity of active substance used as a starting material in veterinary medicinal products returned;

    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)

  16. #2116095

    ciallaíonn “substaintí gníomhacha falsaithe a úsáidtear mar ábhair thosaigh i dtáirgí íocshláinte tréidliachta” aon substaint ghníomhach a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta a bhfuil léiriú bréagach ann ar aon cheann díobh seo a leanas:

    ‘falsified active substance used as a starting material in veterinary medicinal products’ means any active substance used as a starting material in veterinary medicinal products with a false representation of any of the following:

    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)

  17. #2116233

    I gcás ina bhfuil daoine dá dtagraítear in Airteagal 1(2) den tuairim go mb’fhéidir gur substaint ghníomhach a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta falsaithe í an substaint ghníomhach a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta a soláthraíodh dóibh nó a d'allmhairigh siad, déanfaidh na daoine sin an tsubstaint a leithscaradh go fisiceach nó, má tá córas leictreonach coibhéiseach ar fáil, go leictreonach agus cuirfidh siad údarás inniúil náisiúnta an Bhallstáit ina bhfuil siad cláraithe ar an eolas.

    Where persons referred to in Article 1(2) suspect that an active substance used as а starting material in veterinary medicinal products procured or imported by them is a falsified active substance used as а starting material in veterinary medicinal products, they shall segregate it physically or, if an equivalent electronic system is available, electronically and inform the national competent authority of the Member State in which they are registered.

    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)

  18. #304461

    (ii) nádúr na n-oibríochtaí a dhéantar ina n-úsáidtear seachtháirgí ainmhithe nó táirgí díorthaithe mar ábhar tosaigh.

    (ii) the nature of the operations performed using animal by-products or derived products as starting material.

    Regulation (EC) No 1069/2009 of the European Parliament and of the Council of 21 October 2009 laying down health rules as regards animal by-products and derived products not intended for human consumption and repealing Regulation (EC) No 1774/2002 (Animal by-products Regulation)

  19. #717430

    I gcásanna mar sin, bheadh an t-ábhar tosaigh ag an gcéim a thagann roimh an snáth go hiondúil — is í sin an chéim snáithíní.

    In such cases, the starting material would normally be at the stage before yarn — that is the fibre stage.

    Regulation (EU) 2016/1076 of the European Parliament and of the Council of 8 June 2016 applying the arrangements for products originating in certain states which are part of the African, Caribbean and Pacific (ACP) Group of States provided for in agreements establishing, or leading to the establishment of, economic partnership agreements

  20. #1736102

    Maidir le meáin saothrúcháin arb é atá iontu roinnt comhpháirteanna a úsáidtear chun an tsubstaint ghníomhach a tháirgeadh, measfar gur ábhar tosaigh amháin iad.

    Culture media consisting of several components used for production of the active substance shall be regarded as one starting material.

    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)

  21. #1736135

    Cuirfear ar chumas an údaráis inniúil, nuair is gá, samplaí den ábhar tosaigh bitheolaíoch nó imoibrithe a úsáidtear sna nósanna imeachta tástála a chur ar chumas an údaráis inniúil na tástálacha a dhéanfar a sheiceáil.

    When required, samples of the biological starting material or reagents used in the testing procedures shall be provided to enable the competent authority to arrange for check tests to be carried out.

    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)

  22. #1736138

    déanfar ainm an ábhair thosaigh, a chomhlíonann ceanglais phointe 2 de Roinn A, a ionadú le haon chomhchiallaigh thrádála nó eolaíocha,

    the name of the starting material meeting the requirements of point 2 of Section A shall be supplemented by any trade or scientific synonyms,

    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)

  23. #1736139

    an tuairisc ar an ábhar tosaigh, atá leagtha síos i bhfoirm atá cosúil leis an tuairisc a úsáidtear in ítim thuairisciúil in Pharmacopoeia Eorpach,

    the description of the starting material, set down in a form similar to that used in a descriptive item in the European Pharmacopoeia,

    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)

  24. #1736142

    aon réamhchúraimí speisialta a d’fhéadfadh a bheith riachtanach le linn stóráil an ábhair tosaigh, agus, más gá, tabharfar a shaol stórála.

    any special precautions which may be necessary during storage of the starting material and, if necessary, its storage life shall be given.

    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)

  25. #1736217

    Déanfar scrúdú ar fheidhmíocht atáirgthe a mheas nuair a thugann na sonraí le fios b’fhéidir gur riosca féideartha é an t-ábhar tosaigh as a dtagann an táirge.

    Examination of reproductive performance shall be considered when data suggest that the starting material from which the product is derived may be a potential risk factor.

    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)

  26. #1911936

    teorainneacha sonraíochta substainte gníomhaí a ghéarú, ábhar tosaigh, idirmheánach nó imoibrí a úsáidtear i modh monaraíochta na substainte gníomhaí

    tightening of specification limits of an active substance, starting material, intermediate or reagent used in the manufacturing process of the active substance

    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)

  27. #1912122

    Ní chuimseofar i modh monaraíochta na substainte gníomhaí, san ábhar tosaigh, san imoibrí, san idirmheánach ná sa támhán úsáid ábhar de bhunús daonna ná de bhunús ainmhíoch.

    The manufacturing process of the active substance, starting material, reagent, intermediate or excipient shall not include the use of material from human or animal origin.

    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)

  28. #2050006

    Aon réamhchúraim speisialta a d’fhéadfadh a bheith riachtanach le linn stóráil an ábhair tosaigh, agus, más gá, tabharfar a shaol stórála.

    Any special precautions which may be necessary during storage of the starting material and, if necessary, its storage life shall be given.

    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)

  29. #2050013

    Nuair is gá, soláthrófar samplaí den ábhar tosaigh bitheolaíoch nó imoibrithe a úsáidtear sna nósanna imeachta tástála chun a chur ar a chumas don údaráis inniúil na tástálacha a dhéanfar a sheiceáil.

    When required, samples of the biological starting material or reagents used in the testing procedures shall be provided to enable the competent authority to arrange for check tests to be carried out.

    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)

  30. #2050015

    déanfar ainm an ábhair tosaigh, a comhlíonann na ceanglais i bpointe IIIa.2A1(4) a ionadú le haon chomhchiallach trádála nó eolaíoch atá air;

    the name of the starting material meeting the requirements of point IIIa.2A1(4) shall be supplemented by any trade or scientific synonyms;

    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)

  31. #2050016

    an tuairisc ar an ábhar tosaigh, atá leagtha síos i bhfoirm atá cosúil leis an tuairisc a úsáidtear in ítim thuairisciúil in Pharmacopoeia Eorpach;

    the description of the starting material, set down in a form similar to that used in a descriptive item in the European Pharmacopoeia;

    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)

  32. #2050019

    aon réamhchúraim speisialta a d’fhéadfadh a bheith riachtanach le linn stóráil an ábhair tosaigh, agus, más gá, tabharfar a shaol stórála.

    any special precautions which may be necessary during storage of the starting material and, if necessary, its storage life shall be given.

    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)

  33. #2113353

    ciallaíonn “baisc” cainníocht shainithe d’ábhar tosaigh, d’ábhar pacáistithe nó de tháirge a phróiseáiltear in aon phróiseas amháin nó i sraith próiseas, ionas go mbeidh súil leis gur rud aonchineálach é;

    ‘batch’ means a defined quantity of starting material, packaging material or product processed in a single process or series of processes, so that it is expected to be homogeneous;

    Commission Implementing Regulation (EU) 2021/1248 of 29 July 2021 as regards measures on good distribution practice for veterinary medicinal products in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  34. #2116086

    ciallaíonn “baisc” cainníocht shainithe d’ábhar tosaigh, d’ábhar pacáistíochta nó de tháirge a phróiseáiltear in aon phróiseas amháin nó i sraith próiseas, ionas go mbeidh súil leis gur rud aonchineálach é;

    ‘batch’ means a defined quantity of starting material, packaging material or product processed in a single process or series of processes, so that it is expected to be homogeneous;

    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)

  35. #2116087

    ciallaíonn “dáta atástála” an dáta ar cheart athscrúdú a dhéanamh ar shubstaint ghníomhach a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta lena áirithiú go bhfuil sí fós oiriúnach lena húsáid;

    ‘retest date’ means the date when an active substance used as a starting material in veterinary medicinal products should be re-examined to ensure that it is still suitable for use;

    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)

  36. #2116278

    cineál an ghearáin, lena n-áirítear ainm agus baiscuimhir na substainte gníomhaí a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta is ábhar an ghearáin sin;

    nature of the complaint, including name and batch number of the active substance used as a starting material in veterinary medicinal products which is the subject of that complaint;

    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. #2116292

    go bhfuil an tsubstaint ghníomhach a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta ina bunchoimeádáin nár osclaíodh leis na bunshéalaí slándála go léir ann agus bail mhaith uirthi;

    the active substance used as a starting material in veterinary medicinal products is in its original unopened containers with all original security seals present and is in good condition;

    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)

  38. #2116293

    go léirítear leis an bhfaisnéis i scríbhinn a chuir an custaiméir ar fáil go ndearnadh an tsubstaint ghníomhach a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta a stóráil agus a láimhseáil faoi dhálaí cuí;

    it is demonstrated by written information provided by the customer that the active substance used as a starting material in veterinary medicinal products has been stored and handled under proper conditions;

    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)

  39. #2116295

    gur duine atá oilte agus údaraithe chuige sin a rinne an tsubstaint ghníomhach a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta a scrúdú agus a mheasúnú;

    the active substance used as a starting material in veterinary medicinal products has been examined and assessed by a person trained and authorised to do so;

    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)

  40. #2116306

    úsáid nó diúscairt na substainte gníomhaí a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta a cuireadh ar ais agus taifid ar an measúnú a rinneadh.

    use or disposal of the returned active substance used as a starting material in veterinary medicinal products and records of the assessment performed.

    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)

  41. #2116311

    Beidh nós imeachta i bhfeidhm lena sainítear na himthosca faoina ndéanfar aisghairm ar shubstaint ghníomhach a úsáidtear mar ábhar tosaigh i dtáirgí íocshláinte tréidliachta a mheas.

    There shall be a procedure in place that defines the circumstances under which a recall of an active substance used as a starting material in veterinary medicinal products shall be considered.

    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)

  42. #2512359

    ciallaíonn ‘ábhar tosaigh’ substaintí a úsáidtear i bpróiseas monaraíochta an MPCA mar a mhonaraítear é mar shubstráit agus/nó mar oibreán maolánaithe;

    starting material’ means substances used in the manufacturing process of the MPCA as manufactured as substrate and/or buffering agent;

    Commission Regulation (EU) 2022/1439 of 31 August 2022 amending Regulation (EU) No 283/2013 as regards the information to be submitted for active substances and the specific data requirements for micro-organisms (Text with EEA relevance)

  43. #2512984

    ciallaíonn ‘ábhar tosaigh’ substaintí a úsáidtear i bpróiseas monaraíochta an MPCA mar a mhonaraítear é mar fhoshraith agus/nó mar oibreán maolánaithe;

    starting material” means substances used in the manufacturing process of the MPCA as manufactured as substrate and/or buffering agent;

    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)

  44. #2513951

    ciallaíonn ‘ábhar tosaigh’ substaintí a úsáidtear i bpróiseas monaraíochta an MPCA mar a mhonaraítear é mar fhoshraith agus/nó mar oibreán maolánaithe;

    starting material’ means substances used in the manufacturing process of the MPCA as manufactured as substrate and/or buffering agent;

    Commission Regulation (EU) 2022/1441 of 31 August 2022 amending Regulation (EU) No 546/2011 as regards specific uniform principles for evaluation and authorisation of plant protection products containing micro-organisms (Text with EEA relevance)

  45. #2827604

    Tá gá leis sin chun críoch an Aontais a chosaint ón lotnaid shonraithe, toisc gurb iad na síolta sonraithe is ábhar tosaigh le haghaidh na bplandaí uile i gceist.

    This is necessary for the protection of the Union territory from the specified pest, as the specified seeds are the starting material for the production of all respective plants.

    Commission Implementing Regulation (EU) 2023/1032 of 25 May 2023 establishing measures to prevent the introduction into and the spread within the Union territory of Tomato brown rugose fruit virus (ToBRFV) and amending Implementing Regulation (EU) 2020/1191

  46. #304008

    Tá ábhar tosaigh de bhunadh ainmhíoch a d’fhéadfaí a úsáid chun na táirgí díorthaithe dá dtagraítear a mhonarú á rialáil leis na Treoracha sonracha sin cheana féin agus déantar coinníollacha áirithe a fhorchur lena áirithiú go gcosnófar an tsláinte phoiblí agus sláinte ainmhithe.

    Those specific Directives already regulate starting material of animal origin which may be used for the manufacture of the derived products referred to and impose certain conditions to ensure the protection of public or animal health.

    Regulation (EC) No 1069/2009 of the European Parliament and of the Council of 21 October 2009 laying down health rules as regards animal by-products and derived products not intended for human consumption and repealing Regulation (EC) No 1774/2002 (Animal by-products Regulation)

  47. #304650

    2. Ar mhaithe le foinsiú sábháilte, cuirfidh oibreoirí doiciméadacht maidir le ceanglais mhír 1 ar fáil, lena n-áireofar, i gcás inar gá, cruthúnas maidir le sábháilteacht na mbeart bithshlándála a ghlactar chun eascairt rioscaí do shláinte an duine agus do shláinte ainmhithe ó ábhar tosaigh a eisiamh.

    2. For the purpose of safe sourcing, operators shall provide documentation of the requirements of paragraph 1, including, where necessary, proof of the safety of bio-security measures taken in order to exclude risks arising to public and animal health from starting material.

    Regulation (EC) No 1069/2009 of the European Parliament and of the Council of 21 October 2009 laying down health rules as regards animal by-products and derived products not intended for human consumption and repealing Regulation (EC) No 1774/2002 (Animal by-products Regulation)

  48. #1735126

    Chun a fhíorú an bhfuil na sonraí a chuirtear isteach chun deimhniú oiriúnachta a fháil ag comhlíonadh mhonagraif Pharmacopoeia Eorpach, féadfaidh an comhlacht um chaighdeánú le haghaidh ainmníochtaí agus noirm cháilíochta, de réir bhrí an Choinbhinsiúin ar fhorbairt Pharmacopoeia Eorpach arna glacadh le Cinneadh 94/358/CE (an Stiúrthóireacht Eorpach um Cháilíocht Leigheasra agus Cúraim Sláinte (“EDQM”)), féadfaidh sé iarraidh ar an gCoimisiún nó ar an nGníomhaireacht cigireacht arna déanamh ag údarás inniúil a iarraidh i gcás ina bhfuil an t-ábhar tosaigh lena mbaineann faoi réir monagraf de chuid Pharmacopoeia Eorpach.

    In order to verify whether the data submitted for obtaining a certificate of suitability complies with the monographs of the European Pharmacopoeia, the standardisation body for nomenclatures and quality norms within the meaning of the Convention on the elaboration of a European Pharmacopoeia accepted by Council Decision 94/358/EC (European Directorate for the Quality of Medicines and Healthcare (‘EDQM’)) may ask the Commission or the Agency to request an inspection by a competent authority when the starting material concerned is subject to a European Pharmacopoeia monograph.

    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)

  49. #1735583

    I gcás ina bhfuil Deimhniúchán Oiriúnachta d’ábhar tosaigh, do shubstaint ghníomhach nó do thámhán eisithe ag an Stiúrthóireacht Eorpach um Cháilíocht Leigheasra agus Cúraim Sláinte, beidh an Deimhniúchán sin ina thagairt don mhonagraf ábhartha de Pharmacopoeia Eorpach.

    Where a Certificate of Suitability has been issued by the European Directorate for the Quality of Medicines and HealthCare for a starting material, active substance or excipient, this Certificate constitutes the reference to the relevant monograph of the European Pharmacopoeia.

    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)

  50. #1735661

    Áireofar sa chur síos ar an ábhar tosaigh an straitéis mhonaraíochta, nósanna imeachta íonghlanta/díghníomhaithe agus a mbailíochtú agus gach nós imeachta le linn próisis chun cáilíocht, sábháilteacht agus aonchineálacht ó bhaisc go baisc den táirge críochnaithe a áirithiú.

    The description of the starting material shall include the manufacturing strategy, purification/inactivation procedures with their validation and all in-process control procedures designed to ensure the quality, safety and batch to batch consistency of the finished product.

    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)