Примери за използване на Review programme на Английски и техните преводи на Български
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The Review Programme.
Some of the combinations are already supported in the Review Programme but others are not.
The Review Programme.
The list will contain the combinations not currently supported in the Review Programme.
The Review Programme is foreseen to be completed by 2024.
Shetland(MNCR Sector 1)has been studied as part of the Marine Nature Conservation Review programme.
A prospective participant in the Review Programme may join or replace an existing participant by mutual agreement, provided that.
It is an existing active substance(already on the market on 14 May 2000)and is in the Review Programme.
Participants may withdraw from the Review Programme by informing the Agency through R4BP 4 of their intention to withdraw.
The sealochs of the Clyde Sea(MNCR Sector 12) have been studied as part of the Marine Nature Conservation Review programme.
The review programme is a Commission work programme for reviewing all existing biocidal active substances.
The sealochs of Western Scotland(MNCR Sector 13)have been studied as part of the Marine Nature Conservation Review programme.
The substance will continue to be evaluated in the Review Programme(for the relevant product-types) under the newly defined substance identity.
It has been authorised for marketing in the country where you intend to supply it orthat the active substance in the product is in the Review Programme.
The Review Programme is the name commonly used for the work programme for the examination of existing biocidal active substances contained in biocidal products.
The provisions in the BPR will also apply to the applications submitted under the review programme of active substances under the Biocidal Products Directive.
For example, active substances under the Review Programme and biocidal products containing these active substances can be placed on the market while awaiting the final decision on the approval.
This measure has been taken to describe more consistently the precursors andin situ active substance generation combinations covered by the existing entries in the Review Programme.
The newly redefined entries will replace the old entries in the list of substances in the Review Programme and consequently, in the list of active substances and suppliers(Article 95 list).
The active substance approval application must be submitted by the participants within 2 years of the relevant notification compliance decision(in accordance with Article 3(2) of the Review Programme Regulation).
Exception: If the active substance is not yet approved but is in the Review Programme, the biocidal product can be made available on the market and used, subject to national laws.
The Commission in consultation with Member States andparticipants has redefined the identity of active substances included in the Review Programme which can be generated in situ.
The detailed rules for the Review Programme have been adapted to the provisions of the BPR in the new Review Programme Regulation(EU) No 1062/2014, which repeals and replaces Commission Regulation(EC) No 1451/2007.
The table below(fourth column)is a non-exhaustive list of the active substances included in the Review Programme which can be generated in situ and for which new notifications can be made.
In addition, the Review Programme Regulation adapts the processes for the evaluation of a dossier to align them to those described in the BPR for new active substances or in Regulation(EU) No 88/2014 for the amendment of Annex I.
I should like to say that the European Commission is prepared to accept the compromise package, especially the point relating to the need to extend the transitional period by four years instead of three andthe point relating to the two-year limitation on any further extensions, in order to facilitate the review programme.
To ensure that no substance is unduly maintained or included in the Review Programme without subsequently being evaluated, interested companies have twelve months to make a notification of essential data regarding the substance.
In practice, this means that for theadditional precursor(s)/active substance/product type(PT) combinations that are introduced as a result of the redefinition of the in situ generated active substances currently in the review programme the deadline of 1 September 2015 will not apply, and the obligations under Article 95 will only apply at a later date i.e.
As the current state of progress in the review programme of this directive will not allow it to be completed by 2010 as planned, it has become necessary to make the appropriate amendments so that the transitional periods for the most delayed cases can be extended.
ECHA also maintains close cooperation with the Commission's Joint Research Centre(JRC)with regard to issues including the risk assessment of nanomaterials; the Review Programme on the risk assessment of Biocides; and activities on the development and validation of alternatives to animal testing.