Licence applications must relate to at least 10 tonnes and to a maximum of 25 % of the quantity available for the product concerned for the period as specified in Article 2 for which the application for a licence is lodged;

Visa and residence permit applications of employees and their family members shall be granted priority treatment.

In the application for the issue of an operating permit shall be stated and proved with documents the capacities for performing the intended activities and a time proposed for inspection prior to the issue of an operating permit.

In the application for the issue of the operating permit and entry in the record of airports shall be stated and proved with documents the capacity to perform the intended activities and a time of inspection proposed prior to the issue of the operating permit.

On receipt of applications for operating authorisation from an air carrier of one of the Contracting Parties, the competent authorities of the other Party shall grant appropriate authorisations with minimum procedural delay, provided that:

(4) In the case of plans which are the direct basis for the issuing of a construction permit or other permit for an activity affecting the environment, the application of intent must include a cartographic representation at a scale of at least 1:

(3) In the case of the lodging of a request for the stipulation of guidelines for the formulation of the project for acquiring the building permit, the application for the issue of a building permit shall be deemed to be complete only on the day the project for acquiring the building permit is submitted with the prescribed elements.

When granting requested authorisations and permissions to an air carrier on receipt of applications to operate charters and other non-scheduled flights, the Parties shall act with minimum procedural delay.

The Joint Committee set up under Article 14 hereof decides on the form the application for authorization takes and the supporting documents required, as well as on environmental, safety and other conditions for the issue of an authorization.

Applications for authorisation

Submission of licence applications and issue of licences in May 2004

SECTION 1 Requirements for applications for authorisation of genetically modified food and feed

For the purpose of implementing Article 47 of Regulation (EC) No 1829/2003, the Commission shall, on 18 April 2004, publish a list of the genetically modified material that has benefited from a favourable opinion from the Community Scientific Committee(s) or the Authority before that date and for which an application for authorisation has not been rejected in accordance with the relevant Community legislation.

the granting of an authorisation or the rejection of an application for authorisation for material included in the list, in accordance with the relevant Community legislation;

(2) A component part of a petition for the issuing of a license is a projection of the operation and a report on the environmental impact of the operation.

One or more mock-ups of the outer packaging and the immediate packaging of a medicinal product, together with the draft package leaflet, shall be submitted to the authorities competent for authorising marketing when the marketing authorisation is requested.

The person concerned shall be officially notified of any decision to refuse the issue or renewal of a residence permit or to expel him from the territory.

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.

shall check that the documentation submitted in support of the application complies with Articles 12 to 13d and ascertain whether the conditions for the issue of the marketing authorisation have been fulfilled;

(6) If the application refers to the issue of the licence to provide auditing services, the Institute shall issue a ruling from paragraph 3 of this Article within two months of receipt of the application, and in all other cases within 30 days of receipt of the application.

(6) If the request concerns the issue of an authorisation to provide banking activities or for a merger, the Bank of Slovenia must issue the decision under the third paragraph of this article within two months from the receipt of the request, and, in all other cases, within thirty days after the receipt of the request.

With a view to the granting of a marketing authorisation for a veterinary medicinal product in more than one Member State, the applicant shall submit an application based on an identical dossier in those Member States.

The competent authorities shall establish a provisional specific allocation for each non-traditional operator registered with them by multiplying the quantity in each operator's application by a coefficient of 0,29 with a view to issuing licences in May 2004.

If the conditions laid down in Article 3(2) or those referred to in Article 3(3) are not satisfied, the competent authorities of the Member State of establishment shall reject an application for the issue or renewal of a Community authorisation or of a driver attestation, by means of a decision which states the reasons therefor.

Following the granting of a marketing authorisation, the authorisation holder may allow use to be made of the pharmaceutical, pre-clinical and clinical documentation contained in the file on the medicinal product, with a view to examining subsequent applications relating to other medicinal products possessing the same qualitative and quantitative composition in terms of active substances and the same pharmaceutical form.";

Without prejudice to Article 5(3) and (5) and Article 17(3) and (5) of Regulation (EC) No 1829/2003, and taking into account the guidance of the European Food Safety Authority (the Authority) provided for in Articles 5(8) and 17(8) of that Regulation, applications for authorisation submitted in accordance with Articles 5 and 17 of Regulation (EC) No 1829/2003 (the applications) shall comply with the requirements of paragraphs 1 to 4 of this Article and with Articles 3 and 4 of this Regulation.

Where a request submitted under Article 4 of Directive 70/524/EEC, concerning products referred to in Article 15(1) of Regulation (EC) No 1829/2003, is supplemented by an application under Regulation (EC) No 1829/2003, in accordance with Article 46(5) of that Regulation, the Member State acting as rapporteur shall ask the applicant without delay to submit a separate application for authorisation in accordance with Article 17 of Regulation (EC) No 1829/2003.

This chapter provides detailed rules concerning applications for authorisation submitted in accordance with Articles 5 and 17 of Regulation (EC) No 1829/2003, including applications submitted under other Community legislation which are transformed or supplemented in accordance with Article 46 of that Regulation.

After the marketing authorisation has been granted, the marketing authorisation holder may allow use to be made of the pharmaceutical, safety and residues, pre-clinical and clinical documentation contained in the file for the veterinary medicinal product with a view to examining a subsequent application for a veterinary medicinal product having the same qualitative and quantitative composition in active substances and the same pharmaceutical form.

If two or more applications submitted in accordance with Articles 12 to 14 have been made for marketing authorisation for a particular veterinary medicinal product and Member States have adopted divergent decisions concerning the authorisation of that veterinary medicinal product, or suspension or revocation of authorisation, a Member State, or the Commission, or the marketing-authorisation holder may refer the matter to the Committee for Medicinal Products for Veterinary Use, hereinafter referred to as 'the Committee', for the application of the procedure laid down in Articles 36, 37 and 38.

Directive 2001/83/EC(4) requires that applications for authorisation to place a medicinal product on the market have to be accompanied by a dossier containing particulars and documents relating in particular to the results of physico-chemical, biological or microbiological tests as well as pharmacological and toxicological tests and clinical trials carried out on the product and thus proving its quality, safety and efficacy.

Member States may not require the application for authorisation to be examined in terms of the economic needs of the market.

LICENCE APPLICATION AND ISSUING FORMALITIES

Examination of applications and issue of a residence permit

CONDITIONS GOVERNING APPLICATIONS FOR AND THE ISSUING OF FISHING LICENCES

In permits and certificates, as well as in applications for the issue of such documents:

(c) in the case of an application for renewal of an authorisation, the authorisation conditions have not been met;

The terms governing the application for and issue of licences are set out in Annex IV.

permits issued pending examination of an application for a residence permit or for asylum.

Applications for authorisations referred to in paragraph 1 shall contain the following information:

permits issued pending examination of an application for a residence permit or for asylum;

2. Applications for authorisations referred to in paragraph 1 shall contain the following information:

Applications for authorisation of new primary products may also be submitted during the first phase.

Fishing licences shall be issued within thirty (30) working days of submission of applications.

Any quantities of a tranche not covered by licence applications shall be carried over to the next tranche.

The procedure for applications for, and issue of, the licences enabling Community vessels to fish in Mozambique's waters shall be as follows:

Without prejudice to Article 8(2), the following information should be included in the application for authorisation referred to in Article 7:

Applications for authorization shall include a description of the plant containing the necessary information for the purposes of the decision whether to grant authorization in accordance with Articles 3 and 4.

The application procedure for, and issue of, the licences enabling Community vessels to fish in the waters of Mauritius shall be as follows:

whereas at the moment no criteria exist for the examination of requests for authorization for use as additives of this new generation of products;