Examples of using Submitted in respect in English and their translations into Polish
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Ecclesiastic
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Financial
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Official/political
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Programming
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Computer
It shall remain applicable to applications submitted in respect of the year 2004.
Applications may be submitted in respect only of animals which on the date of commencement of the retention period are.
Be paid in regard to, and limited to,those areas for which an aid application has been submitted in respect of the final year of the plan;
Only one application may be submitted in respect of a particular type of vehicle, system, component or separate technical unit and in one Member State only.
Comes from straw covered by sale/purchase contracts, processing commitments or processing contracts as referred to in Article 5 covering parcels under flax or hemp grown for fibre and by"area" aid applications as referred to in Article 4 of Regulation(EEC)No 3887/92 submitted in respect of the marketing year concerned, and.
Applications should normally be submitted in respect of the slaughter premium.
The assessment of the dossier submitted in respect of the coccidiostat"Semduramicin sodium" described in the Annex shows that this additive satisfies the above mentioned requirements when used in the animal category and under the conditions described in that Annex.
They shall remain applicable to applications submitted in respect of the 2001 and previous marketing years.
The assessment of the dossier submitted in respect of the authorisation of potassium diformate belonging to the group of"Growth promoters" described in the Annex shows that it satisfies the abovementioned conditions and may therefore be authorised on a provisional basis for a four-year period.
It shall apply to contracts andpayment applications submitted in respect of 2000/2001 and subsequent marketing years.
The assessment of the dossiers submitted in respect of the anti-caking agents"sodium ferrocyanide" and"potassium ferrocyanide" described in Annex I shows that these additives satisfy the abovementioned conditions.
Taking into account the opinion of the SCAN,the assessment of the application for authorisation submitted in respect of the enzyme preparation, shows that the conditions provided for in Article 3a of Directive 70/524/EEC are satisfied.
The assessment of the dossier submitted in respect of the new use of the preparation of enzyme described in Annex III shows that the conditions referred to in Article 9e(1) are satisfied, and the extension of use may therefore be authorised on a provisional basis for a period of four years.
The assessment of the application for an authorisation for a period of 10 years submitted in respect of the coccidiostat preparation,"Sacox 120 microGranulate", shows that the relevant conditions laid down in Directive 70/524/EEC are satisfied.
The assessment of the dossier submitted in respect of the new use of the enzyme preparation described in Annex I shows that it satisfies those conditions and may therefore be authorised on a provisional basis for a four-year period.
For quantities not covered by import licences issued under the September tranche, import licence applications may be submitted in respect of all countries of origin covered by the relevant quota under an additional tranche in October pursuant to Article 4(1), except as regards the quantities set out in paragraph 1(c) above.
New evidence was submitted in respect of the adjustment to the normal value claimed by one exporting producer for a 3% tax paid on imported raw materials purchased on delayed payment terms and which would not be collected in respect of raw materials to be used in the manufacture of SWR to be eventually exported.
The assessment of the application for authorisation submitted, in respect of the acidity regulation preparation"Benzoic acid", shows that the conditions referred to in Directive 70/524/EEC are satisfied.
The assessment of the dossiers submitted in respect of the new uses of the enzyme and micro-organism preparations described in Annexes I and II shows that they satisfy the abovementioned conditions and may therefore be authorised on a provisional basis for a four-year period.
Where, during the period the quotas are opened, the quantities covered by import licence applications submitted in respect of the first, second or third tranches specified in the first paragraph are lower than those available, the remaining quantities shall be added to those available for the following tranche.
The assessment of the dossiers submitted in respect of the new use of the preparations of enzymes described in Annex I and II shows that the conditions referred to in Article 9e(1) are satisfied, and the extensions of use may therefore be authorised on a provisional basis for a period of four years.
The assessment of the application for authorisation submitted in respect of the micro-organism, shows that all the conditions required for an authorisation without a time limit as provided for in Directive 70/524/EEC are satisfied.
Where import licence applications are submitted in respect of rice and broken rice originating in Thailand and rice originating in Australia under the arrangements laid down in Article 1, they shall be accompanied by the original of the export certificate, as shown in Annexes I and II, to be issued by the competent body of the countries indicated therein.
The assessment of the application for authorisation submitted in respect of the new use of this additive, shows that the conditions provided for in Directive 70/524/EEC for provisional authorisation are satisfied.
The assessment of the dossier submitted in respect of the antibiotic preparation described in the Annex to this Regulation, shows that the conditions referred to in Article 3a of the said Directive are satisfied, and the product may therefore be entered in Chapter I of the list of the authorised additives in feedingstuffs pursuant to Article 9t(b) of the said Directive.
Notwithstanding Article 4(2)(a) of Regulation(EEC) No 3887/92,area aid applications submitted in respect of the 2001/02 marketing year and covering holdings complying with all the provisions of Council Regulation(EEC) No 2092/91(13) may be amended to include new areas declared as set-aside.
The assessment of the request for authorisation submitted in respect of manganomanganic oxide shows that this additive, referred to in Article 2(aaaa), meets the requirements laid down in Article 3a of Directive 70/524/EEC, under the conditions set out in the Annex to this Regulation.
To this end, the marketing authorisation holder shall submit a consolidated list of all documents submitted in respect of quality, safety and efficacy, including all variations introduced since the marketing authorisation was granted, at least six months before the marketing authorisation ceases to be valid in accordance with paragraph 1.
The assessments of the applications for authorisation submitted in respect of the new use of the preparations of the enzymes set out in Annex I and II, show that the conditions referred to in Article 9e(1) of Directive 70/524/EEC are satisfied, and the extensions of use should therefore be authorised on a provisional basis for a period of four years.
The assessment of the application for authorisation submitted in respect of that micro-organism preparation, shows that all the conditions required for an authorisation, as provided for in Directive 70/524/EEC are satisfied.