Examples of using Referred to in section in English and their translations into Slovak
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Colloquial
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Official
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Medicine
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Financial
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Ecclesiastic
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Official/political
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Computer
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Programming
The certificate referred to in Section 7.3.
The Online Serviceshall be used by the Users for the purposes referred to in Section 1.
The documentation referred to in Section 4.2.
Applications must be sent no later than the submission deadline referred to in section 3.
The certificate referred to in Section 15.2, and.
People also translate
This is described in the Impact Assessment(LA) referred to in section 1.
The transporter referred to in Section 3 of the journey log shall keep.
The technical documentation referred to in section 2.
For the characteristics referred to in Section 3, the following data shall be reported in physical units:-.
He is subject to the checks referred to in Section 4.
The notified body shall assess the changes proposed and verifywhether after these changes the quality management system still meets the requirements referred to in Section 3.2.
Protective devices as referred to in section 1.4.3, or.
Based on the evaluation report referred to in section 1, two principal problem areas were identified.
The CE mark is accompanied by the identificationsymbol of the notified body responsible for the checks referred to in Section 4.
(a) the identity of the substance(s), as referred to in Section 2 of Annex VI;
Member States shall furnish data for every second year, after the first reference year,for the facilities which are referred to in Section 8(2).
Contributing to the achievement of support programmes as referred to in Section VII of Chapter IV of Title I of this Part.
The buckets shall be sector buckets, as referred to in Section 6, and each bucket shall include all the risk factors allocated to the relevant sector.
He must be subject to the checks referred to in Section 4.
This Appendix sets out the criteria referred to in section 7.1.7 of this Annex regarding the selection of vehicles for testing and the procedures for the in-service conformity control.
Class IIb active devices intended to administer and/or remove a medicinal product, as referred to in Section 6.4 of Annex VIII(Rule 12).
The devices must be designed and manufactured in such a wayas to guarantee the characteristics and performances referred to in Section I on the'General requirements'.
The operator shall crosscheck the information on the label referred to in Section 2 with the information on the accompanying documents.
The notified body must assess the changes proposed and decide whether the altered qualitysystem will still satisfy the requirements referred to in section 3.2 or whether a reassessment is required.
The operator shall crosscheck the information on the label referred to in Section 2 with the information on the accompanying documents.
The budget structure to accommodate the proceeds of the sanctions referred to in Section 4 of Council Regulation(EC) No 1467/97(9) shall be as follows.