Примери за използване на Shall be submitted in accordance на Английски и техните преводи на Български
{-}
-
Colloquial
-
Official
-
Medicine
-
Ecclesiastic
-
Ecclesiastic
-
Computer
They shall be submitted in accordance with the following requirements.
Licence applications referred to in paragraphs 2 and 3 shall be submitted in accordance with Article 12 of Regulation(EC) No 376/2008.
The file shall be submitted in accordance with Annex I and shall contain,in particular, the following information.
To obtain the authorisation referredto in Article 16(2), an application shall be submitted in accordance with the following provisions.
The protocol shall be submitted in accordance with Article 107n(1) of Directive 2001/83/EC.
When reference is made to this Article, an application for authorisation shall be submitted in accordance with the following paragraphs.
Such a report shall be submitted in accordance with the applicable planning and reporting obligations.
Applications for marketing authorisations for the same veterinary medicinal product in two ormore Member States, shall be submitted in accordance with Articles 31 to 43.
Statements of support which have been collected online shall be submitted in accordance with an electronic schema made publicly available by the Commission.
Applications for marketing authorisations for the sameveterinary medicinal product in two or more Member States, shall be submitted in accordance with Articles 31 to 43.
The notification referred to in paragraph 1 shall be submitted in accordance with standard data formats, where they exist under Union law.';
The particulars and documents accompanying the application for marketing authorizationpursuant to Article 8(3)(g) and(h) shall be submitted in accordance with the following requirements.
The request for consent shall be submitted in accordance with Article 9, accompanied by the information mentioned in Article 8(1) and a translation as stated in Article 8(2);
The particulars and documents which must accompany applications for marketing authorization,pursuant to point 3 of Article 8(3)(c) shall be submitted in accordance with the following requirements.
The application shall be submitted in accordance with standard data formats, where they exist pursuant to Article 39f of Regulation(EC) No 178/2002 and accompanied by the following:”;
The particulars and documents which shall accompany the application for marketing authorisation pursuant to the second andfourth indents of Article 12(3)(j) shall be submitted in accordance with the requirements below.
The application shall be submitted in accordance with standard data formats, where they exist pursuant to Article 39f of Regulation(EC) No 178/2002, which shall apply mutatis mutandis.';
Where financial instruments are implemented in accordance with Article 53(3),payment applications that include expenditure for financial instruments shall be submitted in accordance with the following conditions.
An application for the approval of a clinical trial shall be submitted in accordance with national law to a competent authority of the Member State in which the clinical trial is to take place.
As of 1 May 2004,claims for reimbursement relating to the financial contribution for expenditure approved on the basis of Decision 2001/431/EC shall be submitted in accordance with Article 12 of Annex I, part C and Annex II to this Decision.
An application shall be submitted in accordance with Article 7, at the latest one year before the expiry date of the authorisation given pursuant to Directive 70/524/EEC for additives with a limited authorisation period, and within a maximum of seven years after the entry into force of this Regulation for additives authorised without a time limit or pursuant to Directive 82/471/EEC.
For all commitments starting or contracts entering into force after 1 January 2007, payment claims under area-related measures shall be submitted in accordance with the deadlines set out in Article 11(2) of Regulation(EC) No 1122/2009.
The particulars and documents accompanying the application for marketing authorization pursuant to Article 12(3)(i) and(j) and Article 13(1)shall include the results of the tests relating to quality control of all the components used and shall be submitted in accordance with the following provisions.
If the quantity of a notified substance manufactured or imported per manufacturer or importer reaches the next tonnage threshold under Article 12, the additional required information corresponding to that tonnage threshold,as well as to all the lower tonnage thresholds, shall be submitted in accordance with Articles 10 and 12, unless it has already been submitted in accordance with those Articles.
For that purpose, an application shall be submitted to the Agency in accordance with Article 8.
Actions shall be submitted to the Commission in accordance with the detailed rules issued under Article 6.
For this purpose, an application shall be submitted to the Agency in accordance with the provisions of Article 6.
This report shall be submitted to the register for publication in accordance with Article 16.
The request for the opening of group coordination proceedings shall be submitted to the court agreed in accordance with Article 61.
This report shall be submitted to the register for publication in accordance with Article 3 of Directive 68/151/EEC.