Voorbeelden van het gebruik van Inclusion of an active substance in het Engels en hun vertalingen in het Nederlands
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The Directive provides that after inclusion of an active substance in Annex I, Member States must, within a prescribed period,
III to Directive 91/414/EEC set out the requirements for the dossier to be submitted by applicants respectively for the inclusion of an active substance in Annex I and for the authorization of a plant protection product;
III to Directive 91/414/EEC lay down the requirements for the dossier to be submitted by applicants respectively for the inclusion of an active substance in Annex I and for the authorization of a plant protection product;
Whereas Annexes II and III to Directive 91/414/EEC lay down the requirements for the dossier to be submitted by applicants respectively for the inclusion of an active substance in Annex I and for the authorization of a plant protection product;
Annex II to Directive 91/414 contains requirements for the dossier to be submitted for the inclusion of an active substance in Annex I. Annex III contains requirements for the dossier to be submitted for the authorisation of a plant protection product.
Where the Commission decides not to renew the inclusion of an active substance in Annex I, it may grant a period of grace for the disposal,
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;
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.
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;
2002/37 is confirmed by the wording of subsequent directives concerning the inclusion of an active substance in Annex I to Directive 91/414,
IIIB 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
Prior to submitting the opinion on the inclusion or renewal of the inclusion of an active substance in Annex I to the Commission,
In view of ensuring that all proprietary information submitted in support of an inclusion of an active substance or an authorisation of a biocidal product is protected from the moment of its submission
Whereas for these two substances the designated rapporteur Member States have informed the Commission that the notifiers concerned informed them formally that they will not submit the information 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;
Applicants that have invested in supporting the inclusion of an active substance in Annex I or in the authorisation of a biocidal product in accordance with the provisions of this Regulation should be able to recover part of their investment by receiving equitable compensation whenever use of proprietary information which they submitted in support of such inclusions or authorisations is made for the benefit of subsequent applicants.
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.
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.
Renewal and review of an active substance inclusion.
In cases where evaluation of dossiers for the purposes of inclusion of an active substance in Annex I or IA is not completed when the period of three years expires,
The protection period for information submitted in view of the inclusion of an existing active substance in Annex I shall end 10 years from the date of the inclusion of the relevant active substance in Annex I for the particular product-type.