Article 1: Subject matter
Article 2: Scope
Article 3: Definitions
Article 4: Production of controlled substances
Article 5: Placing on the market and use of controlled substances
Article 6: Placing on the market of products and equipment containing or relying on controlled substances
Article 7: Production, placing on the market and use of controlled substances as feedstock
The Commission may determine the form and content of the label to be used. Those measures, designed to amend non-essential elements of this Regulation, inter alia, by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
Article 8: Production, placing on the market and use of controlled substances as process agents
The Commission may determine the form and content of the label to be used. Those measures, designed to amend non-essential elements of this Regulation, inter alia, by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
The maximum amount of controlled substances that may be used as process agents within the Community shall not exceed 1 083 metric tonnes per year.
The maximum amount of controlled substances that may be emitted from process agent uses within the Community shall not exceed 17 metric tonnes per year.
Article 9: Placing on the market of controlled substances for destruction or reclamation and of products and equipment containing or relying on controlled substances for destruction
Article 10: Essential laboratory and analytical uses of controlled substances other than hydrochlorofluorocarbons
The Commission may determine the form and content of the label to be used. Those measures, designed to amend non-essential elements of this Regulation, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
Controlled substances referred to in the first subparagraph shall only be placed on the market and further distributed under the conditions set out in Annex V. The Commission may amend that Annex. Those measures, designed to amend non-essential elements of this Regulation, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
The total quantity annually authorised under licences, including licences for hydrochlorofluorocarbons under Article 11(2), shall not exceed 110 ODP tonnes. Remaining quantities may be allocated to producers and importers which did not place on the market or use controlled substances, for their own account for essential laboratory and analytical uses in the years 2007 to 2009.
The Commission shall determine a mechanism for the allocation of quotas to producers and importers. Those measures, designed to amend non-essential elements of this Regulation, inter alia, by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
The competent authority of the Member State concerned shall notify the Commission in advance of its intention to issue any such authorisation.
The competent authority of the Member State concerned shall notify the Commission in advance of its intention to issue any such authorisation.
Article 11: Production, placing on the market and use of hydrochlorofluorocarbons and placing on the market of products and equipment containing or relying on hydrochlorofluorocarbons
Article 10(3) to (7) shall apply mutatis mutandis.
Undertakings using reclaimed or recycled hydrochlorofluorocarbons for maintenance or servicing shall keep a record of the undertakings that have supplied reclaimed hydrochlorofluorocarbons and of the source of recycled hydrochlorofluorocarbons.
This exemption may not be authorised for a period which extends beyond 31 December 2019.
Article 12: Quarantine and pre-shipment applications and emergency uses of methyl bromide
Methyl bromide may only be used on sites approved by the competent authorities of the Member State concerned and, if economically and technically feasible, subject to the condition that at least 80 % of methyl bromide released from the consignment is recovered.
Each undertaking shall ensure that the calculated level of methyl bromide which it places on the market or uses for its own account for quarantine and pre-shipment applications shall not exceed 21 % of the average of the calculated level of methyl bromide which it placed on the market or used for its own account for quarantine and pre-shipment in the years 2005 to 2008.
Such authorisation shall apply for a period not exceeding 120 days and to a quantity not exceeding 20 metric tonnes and shall specify measures to be taken to reduce emissions during use.
Article 13: Critical uses of halons and decommissioning of equipment containing halons
Those measures, designed to amend non-essential elements of this Regulation, inter alia, by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
Article 14: Transfer of rights and industrial rationalisation
Article 15: Imports of controlled substances or of products and equipment containing or relying on controlled substances
Article 16: Release for free circulation in the Community of imported controlled substances
The quotas referred to in the first subparagraph shall be allocated only for the following substances:
Article 17: Export of controlled substances or of products and equipment containing or relying on controlled substances
Article 18: Licensing of imports and exports
Article 19: Measures for monitoring of illegal trade
Those measures, designed to amend non-essential elements of this Regulation, inter alia, by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
Article 20: Trade with a State not party to the Protocol and a territory not covered by the Protocol
Where the authorities of a territory not covered by the Protocol are in full compliance with the Protocol and have submitted data to that effect as specified in Article 7 of the Protocol, the Commission may decide that some or all of the provisions of paragraph 1 of this Article shall not apply in respect of that territory.
The Commission shall act in accordance with the management procedure referred to in Article 25(2).
Article 21: List of products and equipment containing or relying on controlled substances
Article 22: Recovery and destruction of used controlled substances
Those measures, designed to amend non-essential elements of this Regulation, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
The Commission shall establish an Annex to this Regulation with a list of products and equipment for which the recovery of controlled substances or destruction of products and equipment without prior recovery of controlled substances shall be considered technically and economically feasible, specifying, if appropriate, the technologies to be applied. Any draft measure to establish such an Annex shall be accompanied and supported by a full economic assessment of costs and benefits, taking into account the individual circumstances of Member States.
Those measures, designed to amend non-essential elements of this Regulation, inter alia, by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
The Commission shall evaluate the measures taken by the Member States and may in the light of this evaluation and of technical and other relevant information, as appropriate, adopt measures regarding those minimum qualification requirements.
Those measures, designed to amend non-essential elements of this Regulation, inter alia, by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
Article 23: Leakages and emissions of controlled substances
The equipment or system shall be checked for leakage within 1 month after a leak has been repaired to ensure that the repair has been effective.
Those measures, designed to amend non-essential elements of this Regulation, inter alia, by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
Those measures, designed to amend non-essential elements of this Regulation, inter alia, by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
Article 24: New substances
Those measures, designed to amend non-essential elements of this Regulation, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
Article 25: Committee
The period laid down in Article 4(3) of Decision 1999/468/EC shall be set at 1 month.
Article 26: Reporting by the Member States
Those measures, designed to amend non-essential elements of this Regulation, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
Article 27: Reporting by undertakings
Those measures, designed to amend non-essential elements of this Regulation, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 25(3).
Article 28: Inspection
The Commission shall take appropriate steps to protect the confidentiality of information obtained under this Article.
Article 29: Penalties
Article 30: Repeal
References to the repealed Regulation shall be construed as references to this Regulation and shall be read in accordance with the correlation table set out in Annex VIII.
Article 31: Entry into force
It shall apply from 1 January 2010.
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Footnote p0: This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Strasbourg, 16 September 2009.