(c) whenever the previous issue of an import authorization by the destination country is a requirement for the issue of the export authorization, the entry shall contain the number (if any) and place and date of issue of the import permit issued by the destination country; a copy of this permit shall be retained in compliance with Article 2 (4) of the basic Regulation;

To the extent that the above events do not affect the authorization of a representative appointed under Article 89 of the Regulation, proceedings shall be interrupted only on application by such representative;

If national laws provide for the confidentiality of judicial investigations, communication of information as provided for in this Regulation shall be subject to authorization by the competent judicial authority.

High Authority Decision No 25/67 of 22 June 1967 laying down in implementation of Article 66(3) of the Treaty a regulation concerning exemption from prior authorization (OJ No 154, 14.7.1967, p. 11), as amended by:

The safe harbor principles contain an exception where statute, regulation or case-law create 'conflicting obligations or explicit authorizations, provided that, in exercising any such authorization, an organization can demonstrate that its non-compliance with the principles is limited to the extent necessary to meet the overriding legitimate interests further by such authorization.

The authorizations referred to in the second subparagraph of Article 2 (1) and the second subpararaph of Article 2 (3) shall be granted in accordance with the procedure laid down in Article 24 of Regulation (EEC) No 2759/75.

No medicinal product referred to in Part A of the Annex may be placed on the market within the Community unless a marketing authorization has been granted by the Community in accordance with the provisions of this Regulation.

Without prejudice to technical enforcement measures, the authorization referred to in paragraph 1 above shall be suspended or revoked pursuant to Articles 5 (3) and 5a (3) of the basic Regulation, or refused, in particular, if:

Commission Regulation (EC) No 1662/95 of 7 July 1995 laying down certain detailed arrangements for implementing the Community decision-making procedures in respect of marketing authorizations for products for human or veterinary use

The purpose of this Regulation is to lay down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and to establish a European Agency for the Evaluation of Medicinal Products.

in Article 1, the terms 'Regulation (EC) No 517/94 is hereby amended as follows' shall be replaced by 'In application of Regulation (EC) No 517/94 import authorizations and the extracts shall be issued in accordance with the conditions and conform to the specimen as set out in the Annex.

Whereas, moreover, this Regulation aims at specifying the connection between the Community plant variety right and the rights which derive from the provisions of Article 14 of the basic Regulation, on one hand, and that between the authorization granted to the farmer and his holding, on the other hand;

The person responsible for placing on the market a medicinal product referred to in Part B of the Annex may request that authorization to place the medicinal product on the market be granted by the Community in accordance with the provisions of this Regulation.

In order that a veterinary medicinal product may be the subject of a marketing authorization for the purpose of administering it to food-producing animals, the active substances which it contains must be shown in Annexes I, II or III of Regulation (EEC) No 2377/90.

The competent authorities in the Community shall debit the specific quantitative limits referred to in paragraph 1 at the time of issue of the prior authorization required by Council Regulation (EEC) No 636/82 which governs economic outward processing arrangements.

For the purposes of obtaining a marketing authorization in respect of a veterinary medicinal product, other than under the procedure established by Regulation (EEC) No 2309/93, an application shall be lodged with the competent authority of the Member State concerned.

Article 2 of Council Regulation (EEC) No 3164/76 of 16 December 1976 on the Community quota for the carriage of goods by road between Member States (8), as last amended by Regulation (EEC) No 18 41 / 88 (9), which provides that the Community authorization should be presented at the request of any authorized inspecting officer.

shall verify that the particulars and documents submitted in accordance with Article 28 comply with the requirements of Directives 81/851/EEC and 81/852/EEC and examine whether the conditions specified in this Regulation for issuing a marketing authorization are satisfied;

Any product which, on the date on which this Regulation enters into force, is protected by a valid basic patent and for which the first authorization to place it on the market as a medicinal product in the Community was obtained after 1 January 1985 may be granted a certificate.

when notice of the transaction is published in the Official Journal, pursuant to Article 4 (3) of Council Regulation No 4064/89, or when notice of the transaction is received under Article 66 of the ECSC Treaty and a prior authorization from the Commission is required under that provision,

Article 17 of Council Regulation No 517 / 72 / EEC of 28 February 1972 on the introduction of common rules for regular and special regular services by coach and bus between Member States (4) as last amended by Regulation (EEC) No 1301/78 (5), which provides that the authorization provided for in Article 3 of that Regulation and established by Commission Regulation 1172/72 shall be carried on the vehicle and be produced at the request of any authorized inspecting officer;

Authorizations mentioned in Article 1 of Regulation (EEC) No 2204/90 shall be granted for a period of 12 months, at the request of the undertakings concerned subject to their giving a prior undertaking in writing to accept and comply with the provisions of Article 3 (1) (a) and (b) on the one hand, and (c) on the other, of the aforementioned Regulation.

Where it takes the form of an import authorization this may not be relied upon so as to escape the application of protective measures introduced pursuant to Council Regulation (EEC) No 1927/75 of 22 July 1975 relating to rules for trade with third countries in the processed fruit and vegetable sector.

Articles 17 and 18 of Council Regulation No 516/72/EEC of 28 February 1972 on the introduction of common rules for shuttle services by coach and bus between Member States (1) as last amended by Regulation (EEC) No 2778/78 (2), which provide that the authorization, list of passengers and passenger travel document as defined in the Regulation and established in Commission Regulation (EEC) No 1172/72 (3) shall be carried on the vehicle and be produced at the request of any authorized inspecting officer;

shall verify that the particulars and documents submitted in accordance with Article 6 comply with the requirements of Directives 65/65/EEC, 75/318/EEC and 75/319/EEC, and examine whether the conditions specified in this Regulation for issuing a marketing authorization for the medicinal product are satisfied;

The release for free circulation in the Community of imports subject to the quantitative limits provided for in paragraph 1 shall be subject to the presentation of an import authorization or equivalent document issued by the Member States' authorities in accordance with the procedure set out in this Regulation.

Article 14 (3), fourth indent shall not apply to farmers who continue to use an established variety in accordance with the authorization of Article 14 (1) if, before the entry into force of this Regulation, they have already used the variety for the purposes described in Article 14 (1) without payment of a remuneration;

According to the procedure laid down in Article 30 of Regulation (EEC) No 804/86, the Commission shall determine the conditions under which States shall grant the authorizations and the maximum percentages to be incorporated, on the basis of objective criteria laid down having regard to what is technologically necessary.

Whereas, therefore, pending the inclusion of a third country in the list referred to in Article 11 (1) (a), importers should be able to obtain authorization to import from third countries products shown to comply with production rules and inspection arrangements equivalent to those provided for in Regulation (EEC) No 2092/91,

Unless otherwise specified in this Regulation, the details relating to the exercise of the rights, to the use of the authorizations or to the fulfilment of the obligations shall be governed by the law of the Member State, including its international private law, in which the farmer's holding on which the derogation is used, is located.

Natural or legal persons having their domicile or principal place of business or a real and effective industrial or commercial establishment in the Community may be represented before the Office by an employee, who must file with it a signed authorization for insertion on the files, the details of which are set out in the Implementing Regulation.

For the purpose of applying paragraph 1 (b), special or exclusive rights shall mean rights deriving from authorizations granted by a competent authority of the Member State concerned, by law, regulation or administrative action, having as their result the reservation for one or more entities of the exploitation of an activity defined in paragraph 2.

Whereas a period of 60 days should be allowed before the entry into force of this Regulation in order to allow Member States to make any adjustment which may be necessary to the authorizations to place the veterinary medicinal products concerned on the market which have been granted in accordance with Council Directive 81/851/EEC (3), as amended by Directive 93/40/EEC (4), to take account of the provisions of this Regulation;

Whereas Article 3 (3) of the said Regulation states that a sum equal to the difference between the value of the skimmed milk resulting from the intervention price for skimmed milk powder on the one hand and the market price for casein and caseinates on the other hand, plus 10 %, is due for quantities of caseins and caseinates used without authorization;

Where the Commission, pursuant to Article 12 of this Regulation has confirmed that the amount requested is available within the quantitative limit in question, the authorities of a Member State shall issue an import authorization within a maximum of five working days of the presentation by the importer of the original of the corresponding export licence.

Whereas a period of 60 days should be allowed before the entry into force of this Regulation in order to allow Member States to make any adjustment which may be necessary to the authorizations to place the veterinary medicinal products concerned on the market which have been granted in accordance with Council Directive 81/851/EEC(1), as last amended by Directive 93/40/ EEC (2) to take account of the provisions of this Regulation;

Whereas a period of 60 days should be allowed before the entry into force of this Regulation in order to allow Member States to make any adjustment which may be necessary to the authorizations to place the veterinary medicinal products concerned on the market which have been granted in accordance with Council Directive 81/851/EEC (3), as last amended by Directive 93/40/ EEC (4) to take account of the provisions of this Regulation;

Whereas a period of 60 days should be allowed before the entry into force of this Regulation in order to allow Member States to make any adjustmenmt which may be necessary to the authorizations to place the veterinary medicinal products concerned on the market which have been granted in accordance with Council Directive 81/851/EEC(3), as last amended by Directive 93/40/ EEC (4) to take account of the provisions of this Regulation;

Whereas a period of 60 days should be allowed before the entry into force of this Regulation in order to allow Member States to make any adjustment which may be necessary to the authorizations to place the veterinary medicinal products concerned on the market which have been granted in accordance with Council Directive 81/851/EEC(4), as last amended by Directive 93/40/ EEC (5), to take account of the provisions of this Regulation;

Whereas a period of 60 days should be allowed before the entry into force of this Regulation in order to allow Member States to make any adjustment which may be necessary to the authorizations to place the veterinary medicinal products concerned on the market which have been granted in accordance with Council Directive 81/851/EEC(3), as last amended by Directive 93/40/ EEC (4), to take account of the provisions of this Regulation;

Whereas a period of 60 days should be allowed before the entry into force of this Regulation in order to allow Member States to make any adjustment which may be necessary to the authorizations to place the veterinary medicinal products concerned on the market which have been granted in accordance with Council Directive 81/8 51/EEC (3), as last amended by Directive 93/40/ EEC (4) to take account of the provisions of this Regulation;

Whereas a period of 60 days should be allowed before the entry into force of this Regulation in order to allow Member States to make any adjustment which may be necessary to the authorizations to place the veterinary medicinal products concerned on the market which have been granted in accordance with the Council Directive 81/851/EEC (3), as last amended by Directive 93/40/ EEC (4), to take account of the provisions of this Regulation;

Any product protected by a patent in the territory of a Member State and subject, prior to being placed on the market as a medicinal product, to an administrative authorization procedure as laid down in Council Directive 65/65/EEC(1) or Directive 81/851/EEC (2) may, under the terms and conditions provided for in this Regulation, be the subject of a certificate.

Without prejudice to more specific requirements to be determined on the basis of agreements with countries concerned, exports of scheduled substances in Category 3 are subject to the provisions of Article 4 of the basic Regulation whenever they are destined to an operator established in a country which is listed in Annex 3 to this Regulation for the substance concerned pursuant to Article 5a (2) of the basic Regulation and an open individual authorization cannot be granted pursuant to paragraph 3 of that Article.

If such earlier acts have involved further propagation which was intended within the meaning of Article 16 (a), the authorization of the holder shall be required for any further propagation after the expiry of the second year, in the case of varieties of vine and tree species after the expiry of the fourth year, following the date of entry into force of this Regulation.

Undertakings entitled in the Member State of establishment, in accordance with that Member State's legislation, to carry out road haulage operations on own account, shall be entitled to receive the cabotage authorizations referred to in Article 2 of Regulation (EEC) No 3118/93, under the same conditions as undertakings performing road haulage operations for hire or reward.

'The authorization referred to in point 4 of (f) may not be granted to a spouse not residing in the Netherlands of an employed or self-employed person to whom the provisions of Article 14 (1), Article 14a (1) or Article 17 of the Regulation apply if that spouse, in accordance with the provisions of Netherlands legislation alone, is or was authorized to take out voluntary insurance.';

whereas, however, with a view to avoiding problems for certain operators in the sector, the authorization to use the control attestation should be extended beyond 30 April 1992 for hops originating in countries which are not included in the Annex to Commission Regulation (EEC) No 3077/78 of 21 December 1978 on the equivalence with Community certificates of attestations accompanying hops imported from non-member countries (5), as last amended by Regulation (EEC) No 2238/91(6);

Any person receiving information under the provisions of Articles 8, 9, 10 or 11 shall not, without prior consent of the person who has supplied the information, pass any of this information to another person or use it for any purpose other than for the exercise of the Community plant variety right or for the use of the authorization provided for in Article 14 of the Basic Regulation, respectively.

Whereas the host Member State should consider the cabotage authorization as sufficient evidence that an undertaking is entitled to carry out road haulage operations on own account in accordance with point 4 of the Annex to the First Council Directive of 23 July 1962 on the establishment of common rules for certain types of carriage of goods by road (2), as last amended by Regulation (EEC) No 881/92(3);