2008/409/EC: Commission Decision of 17 April 2008 on the allocation of quantities... (32008D0409)
EU - Rechtsakte: 15 Environment, consumers and health protection

COMMISSION DECISION

of 17 April 2008

on the allocation of quantities of controlled substances allowed for essential uses in the Community in 2008 under Regulation (EC) No 2037/2000 of the European Parliament and of the Council

(notified under document number C(2008) 1403)

(Only the Danish, Dutch, English, Estonian, French, German, Italian, Slovenian and Spanish texts are authentic)

(Text with EEA relevance)

(2008/409/EC)

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Regulation (EC) No 2037/2000 of the European Parliament and of the Council of 29 June 2000 on substances that deplete the ozone layer(1), and in particular Article 3(1) thereof,
Whereas:
(1) The Community has already phased out the production and consumption of chlorofluorocarbons, other fully halogenated chlorofluorocarbons, halons, carbon tetrachloride, 1,1,1-trichloroethane, hydrobromofluorocarbon and bromochloromethane.
(2) Each year the Commission is required to determine essential uses for these controlled substances, the quantities that may be used and the companies that may use them.
(3) Decision IV/25 of the Parties to the Montreal Protocol on Substances that Deplete the Ozone Layer, hereinafter ‘the Montreal Protocol’, sets out the criteria used by the Commission for determining any essential uses and authorises the production and consumption necessary to satisfy essential uses of controlled substances in each Party.
(4) Decision XIX/13 of the Parties to the Montreal Protocol authorises the production in the European Community of 200 tonnes of chlorofluorocarbons (CFCs) in 2008 for the manufacturing and use of Metered-Dose Inhalers (MDIs) qualifying for essential uses of CFCs as defined in Decision IV/25.
(5) Decision XIX/18 of the Parties to the Montreal Protocol authorises the production and consumption necessary to satisfy essential uses of controlled substances listed in Annexes A, B and C (Group II and III substances) of the Montreal Protocol for laboratory and analytical uses as listed in Annex IV to the report of the Seventh Meeting of the Parties, subject to the conditions set out in Annex II to the report of the Sixth Meeting of the Parties, as well as Decisions VII/11, XI/15 and XV/5 of the Parties to the Montreal Protocol. Decision XVII/10 of the Parties to the Montreal Protocol authorises the production and consumption of the controlled substance listed in Annex E of the Montreal Protocol necessary to satisfy laboratory and analytical uses of methyl bromide.
(6) Pursuant to paragraph 3 of Decision XII/2 of the Parties to the Montreal Protocol on measures to facilitate the transition to chlorofluorocarbon-free MDIs, all Member States have notified(2) the United Nations Environment Programme the active ingredients for which chlorofluorocarbons (CFCs) are no longer essential for the manufacture of CFC-MDIs for placing on the market of the European Community.
(7) Article 4(4)(i)(b) of Regulation (EC) No 2037/2000 prevents CFCs from being used and placed on the market unless they are considered essential under the conditions described in Article 3(1) of that Regulation. These non-essentiality determinations have therefore reduced the demand for CFCs used in MDIs that are placed on the market of the European Community. In addition, Article 4(6) of Regulation (EC) No 2037/2000 prevents CFC-MDI products being imported and placed on the market unless the CFCs in these products are considered essential under the conditions described in Article 3(1).
(8) The Commission has published a Notice(3) on the 18 July 2007 to those companies in the Community of 27 Member States that request consideration by the Commission for the use of controlled substances for essential uses in the Community in 2008 and has received declarations on intended essential uses of controlled substances for 2008.
(9) For the purpose of ensuring that interested companies and operators may continue to benefit in due time from the licensing system, it is appropriate that the present decision shall apply from 1 January 2008.
(10) The measures provided for in this Decision are in accordance with the opinion of the Management Committee established by Article 18(1) of Regulation (EC) No 2037/2000,
HAS ADOPTED THIS DECISION:

Article 1

1.   The quantity of controlled substances of Group I (chlorofluorocarbons 11, 12, 113, 114 and 115) subject to Regulation (EC) No 2037/2000 which may be used for essential medical uses in the Community in 2008 shall be 155 460,00 ozone-depleting potential (ODP) kilograms.
2.   The quantity of controlled substances of Group I (chlorofluorocarbons 11, 12, 113, 114 and 115) and Group II (other fully halogenated chlorofluorocarbons) subject to Regulation (EC) No 2037/2000 which may be used for essential laboratory uses in the Community in 2008 shall be 56 213,60 ODP kilograms.
3.   The quantity of controlled substances of Group III (halons) subject to Regulation (EC) No 2037/2000 that may be used for essential laboratory use in the Community in 2008 shall be 418,7 ODP kilograms.
4.   The quantity of controlled substances of Group IV (carbon tetrachloride) subject to Regulation (EC) No 2037/2000 that may be used for essential laboratory uses in the Community in 2008 shall be 150 832,836 ODP kilograms.
5.   The quantity of controlled substances of Group V (1,1,1-trichloroethane) subject to Regulation (EC) No 2037/2000 that may be used for essential laboratory uses in the European Union in 2008 shall be 381,5 ODP kilograms.
6.   The quantity of controlled substances of Group VI (methyl bromide) subject to Regulation (EC) No 2037/2000 that may be used for laboratory and analytical uses in the Community in 2008 shall be 150,00 ODP kilograms.
7.   The quantity of controlled substances of Group VII (hydrobromofluorocarbons) subject to Regulation (EC) No 2037/2000 that may be used for essential laboratory uses in the Community in 2008 shall be 0,96 ODP kilograms.
8.   The quantity of controlled substances of group IX (bromochloromethane) subject to Regulation (EC) No 2037/2000 that may be used for essential laboratory uses in the Community in 2008 shall be 13,368 ODP kilograms.

Article 2

The chlorofluorocarbon metered-dose inhalers listed in Annex I shall not be placed on markets where the Competent Authority has determined chlorofluorocarbons for metered-dose inhalers on those markets to be non-essential.

Article 3

During the period 1 January to 31 December 2008 the following rules shall apply:
1.
The allocation of essential medical use quotas for chlorofluorocarbons 11, 12, 113, 114 and 115 shall be to the companies indicated in Annex II.
2.
The allocation of essential laboratory use quotas for chlorofluorocarbons 11, 12, 113, 114 and 115 and other fully halogenated chlorofluorocarbons shall be to the companies indicated in Annex III.
3.
The allocation of essential laboratory use quotas for halons shall be to the companies indicated in Annex IV.
4.
The allocation of essential laboratory use quotas for carbon tetrachloride shall be to the companies indicated in Annex V.
5.
The allocation of essential laboratory use quotas for 1,1,1-trichloroethane shall be to the companies indicated in Annex VI.
6.
The allocation of laboratory and analytical critical use quotas for methyl bromide shall be to the companies indicated in Annex VII.
7.
The allocation of essential laboratory use quotas for hydrobromofluorocarbons shall be to the companies indicated in Annex VIII.
8.
The allocation of essential laboratory use quotas for bromochloromethane shall be to the companies indicated in Annex IX.
9.
The essential use quotas for chlorofluorocarbons 11, 12, 113, 114 and 115, other fully halogenated chlorofluorocarbons, carbon tetrachloride, 1,1,1-trichloroethane, hydrobromofluorocarbons and bromochloromethane shall be as set out in Annex X.

Article 4

This Decision shall apply from 1 January 2008 and shall expire on 31 December 2008.

Article 5

This Decision is addressed to the following undertakings:
 
Acros Organics bvba
Janssen Pharmaceuticalaan 3A°
B-2440 Geel
 
Airbus France
Service EVICS
BP M6322
Route de Bayonne 316
F-31060 Toulouse Cedex 16
 
Bie & Berntsen
Sandbækvej 7
DK-2610 Rødovre
 
Boehringer Ingelheim GmbH
Binger Straße 173
D-55216 Ingelheim am Rhein
 
Carlo Erba Reactifs-SDS
ZI de Valdonne, BP 4
F-13124 Peypin
 
Chiesi Farmaceutici SpA
Via Palermo 26/A
I-43100 Parma
 
CNRS — Département Galilée
Observatoire de la Côte d'Azur — Siège Social
Boulevard de l'Observatoire, BP 4229
F-06304 Nice Cedex 4
 
Eras Labo
222 RN 90
F-38330 Saint-Nazaire-les-Eymes
 
Harp International
Gellihirion Industrial Estate
Rhondda, Cynon Taff
Pontypridd CF37 5SX
United Kingdom
 
Health Protection Inspectorate-Laboratories
Paldiski mnt 81
EE-10617 Tallinn
 
Honeywell Specialty Chemicals Seelze GmbH
Wunstorfer Straße 40
Postfach 100262
D-30918 Seelze
 
Ineos Fluor Ltd
PO Box 13
The Heath
Runcorn
Cheshire WA7 4QX
United Kingdom
 
Laboratorio Aldo-Union SA
Baronesa de Maldá 73
Espluges de Llobregat
E-08950 Barcelona
 
LGC Standards GmbH
Mercatorstraße 51
D-46485 Wesel
 
Mallinckrodt Baker EMEA
Teugseweg 20
7418 AM Deventer
Nederland
 
Mebrom
Assenedestraat 4
B-9940 Rieme Ertvelde
 
Merck KGaA
Frankfurter Straße 250
D-64271 Darmstadt
 
Mikro+Polo d.o.o.
Zagrebška cesta 22
SI-2000 Maribor
 
Ministry of Defense
Defence Fuel Lubricants and Chemicals Service/Chemical Laboratory
PO Box 10.000
1780 CA Den Helder
Nederland
 
Panreac Química SAU
Pol. Ind. Pla de la Bruguera
C/Garraf 2
E-08211 Castellar del Vallès — Barcelona
 
Sanolabor d.d.
Leskoškova 4
Ljubljana
Slovenia
 
SICOR SpA
Via Terrazzano 77
I-20017 Rho
 
Sigma Aldrich Chimie SARL
80, rue de Luzais
L'Isle d'Abeau Chesnes
F-38297 St-Quentin-Fallavier
 
Sigma Aldrich Company
The Old Brickyard, New Road
Gillingham SP8 4XT
United Kingdom
 
Sigma Aldrich Laborchemikalien GmbH
Wunstorfer Straße 40
D-30926 Seelze
 
Sigma Aldrich Logistik GmbH
Riedstraße 2
D-89555 Steinheim
 
Tazzetti Fluids SRL
Corso Europa n. 600/a
I-10070 Volpiano (TO)
 
Valeas SpA Pharmaceuticals
Via Vallisneri, 10
I-20133 Milano
 
Valvole Aerosol Research Italiana (VARI) SpA — LINDAL Group Italia
Via del Pino, 10
I-23854 Olginate (LC)
 
VWR I.SAS.
201, rue Carnot
F-94126 Fontenay-sous-Bois
Done at Brussels, 17 April 2008.
For the Commission
Stavros
DIMAS
Member of the Commission
(1)  
OJ L 244, 29.9.2000, p. 1
. Regulation as last amended by Commission Decision 2007/540/EC (
OJ L 198, 31.7.2007, p. 35
).
(2)  www.unep.org/ozone/Information_for_the_Parties/3Bi_dec12-2-3.asp
(3)  
OJ C 164, 18.7.2007, p. 37
.

ANNEX I

Pursuant to paragraph 3 of Decision XII/2 of the Twelfth Meeting of the Parties to the Montreal Protocol on measures to facilitate the transition to chlorofluorocarbon-free metered-dose inhalers (MDIs), the following countries have determined that, due to the presence of suitable non-CFC MDIs, CFCs no longer qualify as ‘essential’ under the Protocol when combined with following active ingredients:
LIST OF NON-ESSENTIAL SUBSTANCES
Source:
www.unep.org/ozone/Information_for_the_Parties/3Bi_dec12-2-3.asp
Table 1
Short-acting beta agonist bronchodilators

Country

Salbutamol

Terbutaline

Fenoterol

Orciprenaline

Reproterol

Carbuterol

Hexoprenaline

Pirbuterol

Clenbuterol

Bitolterol

Procaterol

Austria

X

X

X

X

X

X

X

X

X

X

X

Belgium

X

X

X

X

X

X

X

X

X

X

X

Bulgaria

X

X

X

X

X

X

X

X

X

X

X

Cyprus

X

X

X

X

X

X

X

X

X

X

X

Czech Republic

X

X

X

X

X

X

X

X

X

X

X

Denmark

X

X

X

X

X

X

X

X

X

X

X

Estonia

X

X

X

X

X

X

X

X

X

X

X

Finland

X

X

X

X

X

X

X

X

X

X

X

France

X

X

X

X

X

X

X

X

X

X

X

Germany

X

X

X

X

X

X

X

X

X

X

X

Greece

X

X

X

X

X

X

X

X

X

X

X

Hungary

X

X

X

X

X

X

X

X

X

X

X

Ireland

X

X

X

X

X

X

X

X

X

X

X

Italy

X

X

X

X

X

X

X

X

X

X

X

Latvia

X

X

X

X

X

X

X

X

X

X

X

Lithuania

X

X

X

X

X

X

X

X

X

X

X

Luxembourg

X

X

X

X

X

X

X

X

X

X

X

Malta

X

X

X

X

X

X

X

X

X

X

X

Netherlands

X

X

X

X

X

X

X

X

X

X

X

Poland

X

X

X

X

X

X

X

X

X

X

X

Portugal

X

X

X

X

X

X

X

X

X

X

X

Romania

X

X

X

X

X

X

X

X

X

X

X

Slovakia

X

X

X

X

X

X

X

X

X

X

X

Slovenia

X

X

X

X

X

X

X

X

X

X

X

Spain

X

X

X

X

X

X

X

X

X

X

X

Sweden

X

X

X

X

X

X

X

X

X

X

X

United Kingdom

X

X

X

X

X

X

X

X

X

X

X

Table 2
Inhaled steroids

Country

Beclomethasone

Dexamethasone

Flunisolide

Fluticasone

Budesonide

Triamcinolone

Austria

X

X

X

X

X

X

Belgium

X

X

X

X

X

X

Bulgaria

X

X

X

X

X

X

Cyprus

 

 

 

 

 

 

Czech Republic

X

X

X

X

X

X

Denmark

X

 

 

X

 

 

Estonia

X

X

X

X

X

X

Finland

X

 

 

X

 

 

France

X

 

 

X

 

 

Germany

X

X

X

X

X

X

Greece

X

 

X

X

X

X

Hungary

X

X

X

X

X

X

Ireland

X

 

 

X

 

 

Italy

X

X

X

X

X

X

Latvia

X

X

X

X

X

X

Lithuania

X

X

X

X

X

X

Luxembourg

X

X

X

X

X

X

Malta

X

 

 

X

 

 

Netherlands

X

X

X

X

X

X

Poland

X

X

X

X

X

X

Portugal

X

X

X

X

X

X

Romania

X

X

X

X

X

X

Slovakia

X

X

X

X

X

X

Slovenia

X

X

X

X

X

X

Spain

X

 

 

X

X

 

Sweden

X

 

 

X

 

 

United Kingdom

 

 

 

X

 

 

Table 3
Non-steroidal anti-inflammatories

Country

Cromoglicic acid

Nedrocromil

 

 

 

 

Austria

X

X

 

 

 

 

Belgium

X

X

 

 

 

 

Bulgaria

X

X

 

 

 

 

Cyprus

X

X

 

 

 

 

Czech Republic

X

X

 

 

 

 

Denmark

X

X

 

 

 

 

Estonia

X

X

 

 

 

 

Finland

X

X

 

 

 

 

France

X

X

 

 

 

 

Germany

X

X

 

 

 

 

Greece

X

X

 

 

 

 

Hungary

X

 

 

 

 

 

Ireland

 

 

 

 

 

 

Italy

X

X

 

 

 

 

Latvia

X

X

 

 

 

 

Lithuania

X

X

 

 

 

 

Luxembourg

X

 

 

 

 

 

Malta

 

X

 

 

 

 

Netherlands

X

X

 

 

 

 

Poland

X

X

 

 

 

 

Portugal

X

 

 

 

 

 

Romania

X

X

 

 

 

 

Slovakia

X

X

 

 

 

 

Slovenia

X

X

 

 

 

 

Spain

 

X

 

 

 

 

Sweden

X

X

 

 

 

 

United Kingdom

X

X

 

 

 

 

Table 4
Anticholinergic bronchodilators

Country

Ipratropium bromide

Oxitropium bromide

 

 

 

 

Austria

X

X

 

 

 

 

Belgium

X

X

 

 

 

 

Bulgaria

X

X

 

 

 

 

Cyprus

X

X

 

 

 

 

Czech Republic

X

X

 

 

 

 

Denmark

X

X

 

 

 

 

Estonia

X

X

 

 

 

 

Finland

X

X

 

 

 

 

France

 

 

 

 

 

 

Germany

X

X

 

 

 

 

Greece

X

X

 

 

 

 

Hungary

X

X

 

 

 

 

Ireland

X

X

 

 

 

 

Italy

 

 

 

 

 

 

Latvia

X

X

 

 

 

 

Lithuania

X

X

 

 

 

 

Luxembourg

X

X

 

 

 

 

Malta

X

X

 

 

 

 

Netherlands

X

X

 

 

 

 

Poland

X

X

 

 

 

 

Portugal

X

 

 

 

 

 

Romania

X

X

 

 

 

 

Slovakia

X

X

 

 

 

 

Slovenia

X

X

 

 

 

 

Spain

X

X

 

 

 

 

Sweden

X

X

 

 

 

 

United Kingdom

X

X

 

 

 

 

Table 5
Long-acting beta agonist bronchodilators

Country

Formoterol

Salmeterol

 

 

 

 

Austria

X

X

 

 

 

 

Belgium

X

X

 

 

 

 

Bulgaria

X

X

 

 

 

 

Cyprus

X

 

 

 

 

 

Czech Republic

X

X

 

 

 

 

Denmark

 

X

 

 

 

 

Estonia

X

X

 

 

 

 

Finland

X

X

 

 

 

 

France

X

X

 

 

 

 

Germany

X

X

 

 

 

 

Greece

 

 

 

 

 

 

Hungary

X

X

 

 

 

 

Ireland

X

X

 

 

 

 

Italy

X

X

 

 

 

 

Latvia

X

X

 

 

 

 

Lithuania

X

X

 

 

 

 

Luxembourg

X

X

 

 

 

 

Malta

X

X

 

 

 

 

Netherlands

X

X

 

 

 

 

Poland

X

X

 

 

 

 

Portugal

X

X

 

 

 

 

Romania

X

X

 

 

 

 

Slovakia

X

X

 

 

 

 

Slovenia

X

X

 

 

 

 

Spain

 

X

 

 

 

 

Sweden

X

X

 

 

 

 

United Kingdom

X

X

 

 

 

 

Table 6
Combinations of active ingredients in a single MDI

Country

 

 

 

 

 

 

Austria

X All products

 

 

 

 

 

Belgium

X All products

 

 

 

 

 

Bulgaria

X All products

 

 

 

 

 

Cyprus

 

 

 

 

 

 

Czech Republic

X All products

 

 

 

 

 

Denmark

X All products

 

 

 

 

 

Estonia

 

 

 

 

 

 

Finland

X All products

 

 

 

 

 

France

X All products

 

 

 

 

 

Germany

X All products

 

 

 

 

 

Greece

X All products

 

 

 

 

 

Hungary

X All products

 

 

 

 

 

Ireland

 

 

 

 

 

 

Italy

Budesonide + Fenoterol

Fluticasone+ Salmeterol

 

 

 

 

Latvia

X All products

 

 

 

 

 

Lithuania

X All products

 

 

 

 

 

Luxembourg

X All products

 

 

 

 

 

Malta

X All products

 

 

 

 

 

Netherlands

X All products

 

 

 

 

 

Poland

X All products

 

 

 

 

 

Portugal

X All products

 

 

 

 

 

Romania

X All products

 

 

 

 

 

Slovakia

X All products

 

 

 

 

 

Slovenia

X All products

 

 

 

 

 

Spain

 

 

 

 

 

 

Sweden

X All products

 

 

 

 

 

United Kingdom

 

 

 

 

 

 

ANNEX II

ESSENTIAL MEDICAL USES

Quota of controlled substances of Group I that may be used in the production of metered dose inhalers (MDIs) for the treatment of asthma and other chronic obstructive pulmonary diseases (COPDs) are allocated to:
 
Boehringer Ingelheim GmbH (DE)
 
Chiesi Farmaceutici SpA (IT)
 
Laboratorio Aldo Union SA (ES)
 
SICOR SpA (IT)
 
Valeas SpA Pharmaceuticals (IT)
 
(VARI) SpA — LINDAL Group Italia (IT)

ANNEX III

ESSENTIAL LABORATORY USES

Quota of controlled substances of Groups I and II that may be used for laboratory and analytical uses, are allocated to:
 
Bie & Berntsen (DK)
 
Carlo Erba Reactifs-SDS (FR)
 
CNRS — Département Galilée (FR)
 
Harp International (UK)
 
Honeywell Specialty Chemicals (DE)
 
Ineos Fluor (UK)
 
LGC Standards (DE)
 
Mallinckrodt Baker (NL)
 
Merck KGaA (DE)
 
Mikro + Polo (SI)
 
Panreac Quimica (ES)
 
Sanolabor (SI)
 
Sigma Aldrich Chimie (FR)
 
Sigma Aldrich Company (UK)
 
Sigma Aldrich Logistik (DE)
 
Tazzetti Fluids (IT)
 
VWR ISAS (FR)

ANNEX IV

ESSENTIAL LABORATORY USES

Quota of controlled substances of Group III that may be used for laboratory and analytical uses are allocated to:
 
Airbus France (FR)
 
Eras Labo (FR)
 
Ineos Fluor (UK)
 
Ministry of Defence (NL)

ANNEX V

ESSENTIAL LABORATORY USES

Quota of controlled substances of Group IV that may be used for laboratory and analytical uses, are allocated to:
 
Acros Organics (BE)
 
Bie & Berntsen (DK)
 
Carlo Erba Reactifs-SDS (FR)
 
Health Protection Inspectorate-Laboratories (EE)
 
Honeywell Specialty Chemicals (DE)
 
Mallinckrodt Baker (NL)
 
Merck KGaA (DE)
 
Mikro + Polo (SI)
 
Panreac Quimica (ES)
 
Sanolabor d.d. (SI)
 
Sigma Aldrich Chimie (FR)
 
Sigma Aldrich Company (UK)
 
Sigma Aldrich Laborchemikalien (DE)
 
Sigma Aldrich Logistik (DE)
 
VWR ISAS (FR)

ANNEX VI

ESSENTIAL LABORATORY USES

Quota of controlled substances of Group V that may be used for laboratory and analytical uses are allocated to:
 
Acros Organics (BE)
 
Bie & Berntsen (DK)
 
Merck KgaA (DE)
 
Mikro + Polo (SI)
 
Panreac Quimica (ES)
 
Sanolabor d.d. (SI)
 
Sigma Aldrich Chimie (FR)
 
Sigma Aldrich Company (UK)
 
Sigma Aldrich Logistik (DE)

ANNEX VII

LABORATORY AND ANALYTICAL CRITICAL USES

Quota of controlled substances of Group VI that may be used for laboratory and analytical critical uses are allocated to:
 
Mebrom NV (BE)
 
Sigma Aldrich Logistik (DE)

ANNEX VIII

ESSENTIAL LABORATORY USES

Quota of controlled substances of Group VII that may be used for laboratory and analytical uses are allocated to:
Ineos Fluor (UK)

ANNEX IX

ESSENTIAL LABORATORY USES

Quota of controlled substances of Group IX that may be used for laboratory and analytical uses are allocated to:
 
Ineos Fluor (UK)
 
Sigma Aldrich Company (UK)
 
Sigma Aldrich Logistik (DE)

ANNEX X

This Annex is not published because it contains confidential commercial information.
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