Exemple de utilizare a Inclusion of an active substance în Engleză și traducerile lor în Română
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Inclusion of an active substance in Annex I.
Article 11 Procedure for inclusion of an active substance in Annex I, LA or IB.
Inclusion of an active substance in Annex I may be subject to requirements such as.
Providing advice and assistance to applicants for the inclusion of an active substance in Annex I or for a Community authorisation;
Inclusion of an active substance in Annexes I, IA or IB shall, where appropriate, be subject to the following.
Data requirements for an application for the amendment of Annex I to the BPR(first inclusion of an active substance or amendment of restrictions).
Article 10 Inclusion of an active substance in Annexes I, LA or IB.
Where those indications are confirmed,the Commission shall adopt a decision amending the inclusion of an active substance in Annex I or removing it from that Annex.
Fees for inclusion of an active substance in Annex I amount to EUR 400,000.
Whereas for this substance the sole notifier concerned formally submitted to the designated rapporteur Member State information as required pursuant to Article 6(1) of Regulation(EEC)No 3600/92 to support the inclusion of an active substance in Annex I to Directive 91/414/EEC;
For inclusion of an active substance in Annex I, the following shall be taken into particular account.
Whereas for this substance the designated rapporteur Member State has informed the Commission that the notifier concerned informed them formally that they will not submit the information required under Article 6(1) of Regulation(EEC)No 3600/92 to support the inclusion of an active substance in Annex I of Directive 91/414/EEC;
Inclusion of an active substance in Annex I shall be decided in accordance with the procedure laid down in Article 19.
(1) Annexes IIB andIIIB to Directive 91/414/EEC set out the requirements for the dossier to be submitted by an applicant respectively for the inclusion of an active substance consisting of micro-organisms or viruses in Annex I to that Directive and for the authorisation of a plant protection product based on preparations of micro-organisms or viruses.
The inclusion of an active substance in Annex I, IA or IB may be renewed on one or more occasions for periods not exceeding 10 years.
When, on imperative grounds of urgency, the normal time limits for the regulatory procedure with scrutiny cannot be complied with, the Commission should be able to apply the urgency procedure provided for in Article 5a(6)of Decision 1999/468/EC for the adoption of decisions to amend the inclusion of an active substance in Annex I or to remove it from that Annex on basis of Article 13.
The procedure for inclusion of an active substance in Annex I to Directive 91/414 is governed by Article 6 of that directive.
( 7) A notification procedure should be provided by which interested producers have the right to inform the Commission of their interest in securing the inclusion of an active substance in Annex I to Directive 91/414/EEC and of their undertaking to submit all the required information for a proper evaluation of, and decision on, that active substance in the light of the criteria for inclusion set out in Article 5 of Directive 91/414/EEC.
The inclusion of an active substance in Annex I is decided by the Commission- on the basis of risk assessments carried out by the European Food Safety Authority- subject to the opinion of the experts on the Standing Committee on the Food Chain and Animal Health(SCoFCAH).
Whereas a notification procedure has to be provided by which interested producers have the right to inform the Commission of their interest in securing the inclusion of an active substance in Annex I to the Directive and of their undertaking to submit all the requisite information for a proper evaluation of, and decision on, that active substance in the light of the criteria for inclusion set out in Article 5 of Directive 91/414/EEC;
The inclusion of an active substance in Annex I is decided by the Commission- on the basis of risk assessments carried out by the European Food Safety Authority- subject to the opinion of the experts of the Standing Committee on the Food Chain and Animal Health(SCoFCAH).
Article 6(1) provides that the inclusion of an active substance in Annex I is to be decided in accordance with a prescribed procedure.
Where a decision on the inclusion of an active substance in Annex I has not yet been adopted by the Commission when the period of three years expires, the competent authority which granted a provisional authorisation, or the Commission, may extend the provisional authorisation for a period not exceeding one year, provided there are good reasons to believe that the active substance will satisfy the requirements of Article 4.
The applicant shall submit the application for renewal of the inclusion of an active substance in Annex I to the Agency at least 18 months before the expiry of the inclusion in Annex I for a given product-type.
The Commission shall renew the inclusion of an active substance in Annex I if the active substance still complies with the requirements referred to in Article 4.
By way of derogation from Article 6, if, on expiry of the three-year period,a decision has not been taken concerning the inclusion of an active substance in Annex I, a further period may be ordered by the procedure referred to in Article 19 to enable a full examination to be made of the dossier and, where appropriate, of any additional information requested in accordance with Article 6(3) and(4).
(b) an application for inclusion of an active substance in product types other than those for which it is included in the list referred to in paragraph 1(b).
(10) Article 5(5) of the Directive provides that the inclusion of an active substance in Annex I can be reviewed at any time if there are indications that the criteria for inclusion are no longer satisfied.
(7) The Directive provides that after inclusion of an active substance in Annex I, Member States must, within a prescribed period, grant, vary or withdraw, as appropriate, the authorisations of the plant protection products containing the active substance. .
The Commission may review the inclusion of an active substance in Annex I at any time where there are serious indications that the requirements referred to in Article 4 are no longer complied with.