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16 endelig udg. the implementation of council directive 91/676/eØf: gratis på engelsk: europakommissionen, gd
91/676/ety: maksutta, ainoastaan englanniksi: euroopan komissio, po xi, päästä eu:n c02päästötavoitteeseen, joka on 120g/km uusille autoille arvojen tiukentamiseen, eyvl c 259, 1998 (muutetut ehdotukset).
Última atualização: 2014-02-06
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we use a range of assessment tools to make sure we find the candidate whose profile most closely matches the requirements of the position .
we use a range of assessment tools to make sure we find the candidate whose profile most closely matches the requirements of the position .
Última atualização: 2011-10-23
Frequência de uso: 1
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standard operating procedure on referrals in accordance with the provisions of council directive 75/ 319/ eec in the case of safety concerns related to medicinal products marketed in the european union
standard operating procedure on referrals in accordance with the provisions of council directive 75/ 319/ eec in the case of safety concerns related to medicinal products marketed in the european union
Última atualização: 2011-10-23
Frequência de uso: 1
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Aviso: esta concordância pode estar incorreta.
Exclua-a, se este for o caso.
and the documents submitted to us in copy or as specimens conform to the originals .
and the documents submitted to us in copy or as specimens conform to the originals .
Última atualização: 2011-10-23
Frequência de uso: 2
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through this collaboration , it has been possible , for example , to design replacement windows that will be more energy efficient and have a similar profile to the original windows , in line with the requirements of the historic preservation authorities .
through this collaboration , it has been possible , for example , to design replacement windows that will be more energy efficient and have a similar profile to the original windows , in line with the requirements of the historic preservation authorities .
Última atualização: 2011-10-23
Frequência de uso: 1
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vedtaget af bestyrelsen den 18. december 2001 the annual report for 2001 is presented to the management board by the executive director in accordance with article 55( 3) of council regulation (eec) no 2309/ 93.
hallintoneuvosto hyväksyi tämän työohjelman 18. joulukuuta 2001 the annual report for 2001 is presented to the management board by the executive director in accordance with article 55( 3) of council regulation (eec) no 2309/ 93.
Última atualização: 2011-10-23
Frequência de uso: 1
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Aviso: esta concordância pode estar incorreta.
Exclua-a, se este for o caso.
points to consider on the requirements for clinical documentation for metered dose inhalers (mdi) addendum on neuropathic pain to the note for guidance on clinical investigation of medicinal products for nociceptive pain treatment note for guidance on clinical investigation of medical products in the treatment of generalised anxiety disorder note for guidance on clinical investigation of medical products in the treatment of panic disorder.
points to consider on the requirements for clinical documentation for metered dose inhalers (mdi) addendum on neuropathic pain to the note for guidance on clinical investigation of medicinal products for nociceptive pain treatment note for guidance on clinical investigation of medical products in the treatment of generalised anxiety disorder note for guidance on clinical investigation of medical products in the treatment of panic disorder.
Última atualização: 2011-10-23
Frequência de uso: 1
Qualidade:
Aviso: esta concordância pode estar incorreta.
Exclua-a, se este for o caso.
concept paper on the development of an addendum on the clinical requirements of modified release medicinal products submitted as a line- extension of an existing marketing authorisation to the cpmp note for guidance on modified release oral and transdermal dosage forms: section ii (pharmacokinetic and clinical evaluation) (cpmp/ ewp/ 280/ 96)
concept paper on the development of an addendum on the clinical requirements of modified release medicinal products submitted as a line- extension of an existing marketing authorisation to the cpmp note for guidance on modified release oral and transdermal dosage forms: section ii (pharmacokinetic and clinical evaluation) (cpmp/ ewp/ 280/ 96)
Última atualização: 2011-10-23
Frequência de uso: 1
Qualidade:
Aviso: esta concordância pode estar incorreta.
Exclua-a, se este for o caso.
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