The documentation provided shows that those zones meet the requirements of Article 5 of Directive 91/67/EEC.

The documentation provided shows that those farms meet the requirements of Article 6 of Directive 91/67/EEC.

The dossiers submitted appear also to satisfy the data and information requirements of Annex III to Directive 91/414/EEC in respect of one plant protection product containing the active substance concerned.

the documentation provided shall include information on the prevalence and incidence in the Community of the condition for which the medicinal product would be administered at the time at which the application for designation is submitted.

the documentation provided shall include details of any grants, tax incentives or other cost recovery provisions received either within the Community or in third countries;

For this purpose, the documentation provided shall demonstrate that:

(c) the necessary documents are submitted within the time and in the form required;

The deliberations of the panel and the documents submitted to it shall be kept confidential.

- assessments of the effects of plans on the basis of submitted documentation and written sources that are either available or obtained through the suitable methods under the previous indent;

The supporting documents submitted to the Agency shall be sufficient to provide assurance that all the required checks on the eligibility of the claims or invoices authorised for payment have been performed.

The technical regulation shall be listed in the Compendium of Candidates if supported by an affirmative vote in accordance with paragraph 7.1. of Article 7 of Annex B. The documentation submitted with the request for that regulation shall be appended to the listed technical regulation.

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;

If the measurement characteristics of the pattern are known in detail, only an examination of the documents submitted.

17. A 'timely tender' shall be a tender which is submitted to the contractor until the expiration of the deadline as defined in the tender documentation;

They may also communicate other information concerning other prices or values submitted, provided that that is stated in the specifications.

The marketing authorisation shall be refused if the file submitted to the competent authorities does not comply with Articles 12 to 13d and Article 15.

Commission Decision of 6 September 2000 recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of RH-7281 (zoxamide), B-41;

A written agreement must be concluded between the paying agency and that body specifying the nature of the information and the supporting documents to be submitted to the paying agency and the time limit within which they must be submitted;

COMMISSION DECISION of 25 February 2000 recognising in principle the completeness of the dossier submitted for detailed examination with a view to the possible inclusion of spinosad in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market

Commission Decision of 7 June 2000 recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of EXP60707B (acetamiprid) in Annex I to Council Directive 91/414/EEC concerning the placing of plant-protection products on the market

Leaflets shall contain at least the following information, in the order indicated, which shall conform to the particulars and documents provided pursuant to Articles 12 to 13d and the approved summary of product characteristics:";

Furthermore, according to documentary evidence submitted, Indo Pet was able to satisfactorily demonstrate that it did not have any direct or indirect links with any of the Thai exporting producers subject to the anti-dumping measures in force with regard to the product concerned.

Commission Decision of 4 December 2000 recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of UBH 820; UR 50601 (beflubutamid) in Annex I to Council Directive 91/414/EEC concerning the placing of plant-protection products on the market

(4) The jury shall be autonomous in its decisions and opinions. These shall be reached on the basis of projects submitted anonymously, and solely on the grounds of the criteria indicated in the contest notice and in the contract documents in accordance with Article 51 above.

After studying the control reports referred to in Article 81(2), the laboratory responsible for the control shall repeat, on the samples provided, all the tests carried out by the manufacturer on the finished product, in accordance with the relevant provisions shown in the dossier for marketing authorisation.

Commission Decision of 17 July 2000 recognising in principle the completeness of the dossier submitted for detailed examination with a view to the possible inclusion of MKH 65 61 (propoxycarbazone-sodium) in Annex I to Council Directive 91/414/EEC concerning the placing of plant-protection products on the market

COMMISSION DECISION of 23 February 2000 recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of thiacloprid, forchlorfenuron, thiamethoxam in Annex I to Council Directive 91/414/EEC concerning the placing of plant-protection products on the market

Thus, no substantiating evidence, as normally kept in the companies' records, was provided which could have shown that the reported costs of the product concerned were indeed accurate and that such costs reasonably reflected the costs associated with the production and sale of the product concerned.

when no tenders or no suitable tenders or no applications have been submitted in response to an open procedure or a restricted procedure, provided that the initial conditions of contract are not substantially altered and on condition that a report is sent to the Commission if it so requests;

COMMISSION DECISION of 22 July 1999 recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of BAS 656H (dimethenamid-p AC 900001(picolinafen), ZA 1963 (picoxystrobin) in Annex I to Council Directive 91/414/EEC concerning the placing of plant-protection products on the market

At the request of the competent authority of the Member State in which the application is submitted, the competent authority of the other Member State shall transmit, within a period of one month, confirmation that the reference medicinal product is or has been authorised together with the full composition of the reference product and if necessary other relevant documentation.

COMMISSION DECISION of 22 December 1998 recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of CGA 279 202 (trifloxystrobin), clefoxydim (BAS 625H), etoxazol and ferric phosphate in Annex I to Council Directive 91/414/EEC concerning the placing of plant-protection products on the market

However, at any time within 60 days of the date the application for payment is first recorded as received, that period may be interrupted by notifying the contractor concerned that the application is not acceptable because the amount is not due, because the supporting documents required for all additional applications have not been supplied or because the competent body sees the need for further information or checks.

In open procedures, where contracting authorities do not offer unrestricted and full direct access by electronic means in accordance with Article 38(6) to the specifications and any supporting documents, the specifications and supplementary documents shall be sent to economic operators within six days of receipt of the request to participate, provided that the request was made in good time before the deadline for the submission of tenders.

1. if it receives, in an open or restricted procedure, inadequate or unacceptable tenders, while the contents of the tender documentation shall not be basically modified. Contractors shall publish a notice stating that a contract shall be awarded by such procedure save when they have included in the negotiated procedure all tenderers whose tenders had been submitted during the previous open or restricted procedure and complied with the request for recognition of capacity.

may submit the medicinal product, its starting materials and if necessary intermediate products or other constituent materials for testing by an Official Medicines Control Laboratory or a laboratory that a Member State has designated for that purpose, in order to ensure that the testing methods employed by the manufacturer and described in the application documents, in accordance with point (i) of the first subparagraph of Article 12(3), are satisfactory;

List of supporting documents supplied:

The dossiers submitted appear to satisfy also the data and information requirements of Annex III to Directive 91/414/EEC in respect of one plant protection product containing the active substance concerned.

The dossiers submitted appear also to satisfy the data and information requirements of Annex III to Directive 91/414/EEC in respect of one plant-protection product containing the active substance concerned.

The dossiers submitted appear also to satisfy the data and information requirements set out in Annex III to Directive 91/414/EEC in respect of one plant protection product containing the active substance concerned.

ensure that the dossier supplied is in accordance with the requirements of Annex III, at the latest at the time of finalization of the evaluation for the purpose of decision-making, without prejudice, where relevant, to the provisions of Article 13 (1) (a), (4) and (6) of this Directive,

where absence of the contract is justified, documentation is submitted attesting the obligations entered into with the other contracting party or parties, including confirmation from his or their bank of the opening of an irrevocable letter of credit by the purchaser's financial institution to the agreed delivery;

Member States shall examine and verify the validity of the documentation presented.

New Member States shall examine and verify the validity of the documentation presented.

In accordance with the provisions of Article 6(3) of the Directive the Commission confirmed in its Decision 98/ 242/EC fn that the dossier submitted for azafenidin could be considered as satisfying, in principle, the data and information requirements of Annex II and for a plant protection product containing this active substance, of Annex III to the Directive.

Module 2 shall contain a table of contents for the scientific documentation submitted in Modules 2 to 5.

The dossier and the information from the review were also submitted to the Scientific Committee for Plants.

The dossier was referred to the Standing Committee on Plant Health on 5 June 2001.

The dossier was referred to the Standing Committee on Plant Health on 18 October 2000.

However, for other types of minor variations evaluation of the submitted documentation by the Agency should still be required.