Примери за използване на Phase-in substances на Английски и техните преводи на Български
{-}
-
Colloquial
-
Official
-
Medicine
-
Ecclesiastic
-
Ecclesiastic
-
Computer
Specific provisions for phase-in substances.
In the case of phase-in substances, the Agency shall prepare the draft decisions in accordance with Article 40(3).
The last registration deadline of phase-in substances.
Data sharing rules for non-phase-in substances andnot pre-registered phase-in substances.
At the site of injection,the concentration of phase-in substances is stored and creates stocks for the long term.
Participating in a SIEF was a legal obligation for all registrants and pre-registrants of phase-in substances.
In the case of phase-in substances, the competent authority shall prepare the draft decisions in accordance with Article 39(2).
Such substances are called phase-in substances.
Rules for non-phase-in substances and registrants of phase-in substances who have not pre-registered.
All substances that do not fulfil any of the criteria for phase-in substances are considered as non-phase-in substances. .
For phase-in substances there are three examination deadlines(1 December 2012, 1 June 2016 and 1 June 2022) depending on the registration deadlines.
Phase-in substances manufactured in the Community or imported, in quantities reaching 1 000 tonnes or more per year per manufacturer or per importer, at least once after 1 June 2007.
Those non-phase-in substances do not benefit from the transitional regime provided for phase-in substances under REACH and therefore have to be registered before manufacture or import starts.
Manufacturers, importers andonly representatives of non-EEA manufacturers of phase-in substances in quantities of less than one tonne per year who have not pre-registered;
For phase-in substances(see below) that have been imported or manufactured for at least three consecutive years, quantities per year shall be calculated on the basis of the average production or import volumes for the three preceding calendar years.
To benefit from the extended deadlines for registering phase-in substances under the REACH Regulation, registrants have to pre-register their phase-in substances. .
Preparing and submitting an inquiry Before registering, you have a duty to prepare andsubmit an inquiry to ECHA for 1 all non-phase-in substances and 2 phase-in substances….
Potential registrants of phase-in substances that decide to register without pre-registration are mandatory participants of the relevant SIEF once they have registered. They have the obligation to share data they hold on request.
Before registering, you have a duty to prepare andsubmit an inquiry to ECHA for 1 all non-phase-in substances and 2 phase-in substances that have not been pre-registered.
(a) the information specified in Annex VII for non-phase-in substances, and for phase-in substances meeting one or both of the criteria specified in Annex III, manufactured or imported in quantities of one tonne or more per year per manufacturer or importer;
(40) In order to avoid duplication of work, and in particular to avoid duplication of testing,registrants of phase-in substances should pre-register as early as possible with a database managed by the Agency.
For phase-in substances, the manufacturer, importer or downstream user shall comply with this request and with the obligations laid down in Article 14 before the relevant deadline in Article 23 has expired, provided that the downstream user makes his request at least 12 months before the deadline in question.
(b) the information on physicochemical properties specified in Annex VII,section 7 for phase-in substances manufactured or imported in quantities of one tonne or more per year per manufacturer or importer which do not meet either of the criteria specified in Annex III;
The Agency shall undertake thecompleteness check within three weeks of the submission date, or within three months of the relevant deadline of Article 23, as regards registrations of phase-in substances submitted in the course of the two-month period immediately preceding that deadline….
(b) phase-in substances classified as very toxic to aquatic organisms which may cause long-term adverse effects in the aquatic environment(R50/53) in accordance with Directive 67/548/EEC, and manufactured in the Community or imported in quantities reaching 100 tonnes or more per year per manufacturer or per importer, at least once after 1 June 2007;….
EU-based producers or importers of articles should also pre-register those phase-in substances which are intentionally released from their articles, unless the substances were already registered for use in those articles.
Phase-in substance: means a substance which meets at least one of the following criteria.