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Document 32005R0642
Commission Regulation (EC) No 642/2005 of 27 April 2005 imposing testing and information requirements on the importers or manufacturers of certain priority substances in accordance with Council Regulation (EEC) No 793/93 on the evaluation and control of the risks of existing substancesText with EEA relevance
Commission Regulation (EC) No 642/2005 of 27 April 2005 imposing testing and information requirements on the importers or manufacturers of certain priority substances in accordance with Council Regulation (EEC) No 793/93 on the evaluation and control of the risks of existing substancesText with EEA relevance
Commission Regulation (EC) No 642/2005 of 27 April 2005 imposing testing and information requirements on the importers or manufacturers of certain priority substances in accordance with Council Regulation (EEC) No 793/93 on the evaluation and control of the risks of existing substancesText with EEA relevance
OJ L 107, 28.4.2005, p. 14–16
(ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, NL, PL, PT, SK, SL, FI, SV)
OJ L 327M, 5.12.2008, p. 354–358
(MT)
Special edition in Bulgarian: Chapter 15 Volume 013 P. 200 - 202
Special edition in Romanian: Chapter 15 Volume 013 P. 200 - 202
Special edition in Croatian: Chapter 15 Volume 001 P. 149 - 151
In force
28.4.2005 |
EN |
Official Journal of the European Union |
L 107/14 |
COMMISSION REGULATION (EC) No 642/2005
of 27 April 2005
imposing testing and information requirements on the importers or manufacturers of certain priority substances in accordance with Council Regulation (EEC) No 793/93 on the evaluation and control of the risks of existing substances
(Text with EEA relevance)
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Regulation (EEC) No 793/93 of 23 March 1993 on the evaluation and control of risks of existing substances (1), and in particular Article 10(2) thereof,
Whereas:
(1) |
The rapporteurs designated by the Member States in accordance with Article 10(1) of Regulation (EEC) No 793/93 have evaluated the information submitted by the manufacturers and importers in respect of certain priority substances. After consultation of those manufacturers and importers, the rapporteurs have determined that it is necessary for the purposes of the risk evaluation to require those manufacturers and importers to submit further information and carry out further testing. |
(2) |
The information needed to evaluate the substances in question is not available from former manufacturers or importers. The manufacturers and importers have checked that tests on animals cannot be replaced or limited by using other methods. |
(3) |
It is therefore appropriate to request manufacturers and importers of priority substances to submit further information and carry out further testing of those substances. The protocols submitted by the rapporteurs to the Commission should be used for performing those tests. |
(4) |
The provisions of this Regulation are in accordance with the opinion of the Committee established pursuant to Article 15 of Regulation (EEC) No 793/93, |
HAS ADOPTED THIS REGULATION:
Article 1
The manufacturers and importers of the substances listed in the Annex, who have submitted information in accordance with the requirements of Articles 3, 4, 7 and 9 of Regulation (EEC) No 793/93, shall provide the information and perform the tests indicated in the Annex and shall deliver the results to the relevant rapporteurs.
The tests shall be performed according to the protocols specified by the rapporteurs.
The results shall be delivered within the time limits laid down in the Annex.
Article 2
This Regulation shall enter into force on the twentieth day following its publication in the Official Journal of the European Union.
This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 27 April 2005.
For the Commission
Stavros DIMAS
Member of the Commission
(1) OJ L 84, 5.4.1993, p. 1. Regulation as amended by Regulation (EC) No 1882/2003 of the European Parliament and of the Council (OJ L 284, 31.10.2003, p. 1).
ANNEX
No |
Einecs No |
CAS No |
Substance name |
Rapporteur |
Testing/information requirements |
Time limit from the date of entry into force of this Regulation |
|
1 |
201-245-8 |
80-05-7 |
4,4′-Isopropylidenediphenol (1) |
UK |
Long-term fish endocrine effects study with investigation of effects on sperm development |
18 months |
|
Long-term toxicity study with an appropriate freshwater snail species |
18 months |
||||||
2 generation study with 4,4′-isopropylidenediphenol in mice according to OECD 416 (with some specific modifications) |
39 months |
||||||
2 |
203-545-4 |
108-05-4 |
Vinyl acetate (2) |
D |
Further data on pattern of polymerisation facilities and information on exhaust air purification techniques for representative facilities |
6 months |
|
3 |
202-627-7 |
98-01-1 |
2-Furaldehyde (3) |
NL |
Long-term toxicity test with fish |
6 months |
|
Long-term toxicity test with daphnia |
6 months |
||||||
4 |
201-622-7 |
85-68-7 |
Benzyl butyl phthalate (1) |
N |
Data about releases into the Wupper from all sources |
12 months |
|
Plant fumigation test |
12 months |
||||||
Long-term fish study on reproductive and endocrine effects |
12 months |
||||||
Monitoring study on local air concentrations near flooring production sites and sealant formulation plants |
12 months |
||||||
5 |
201-329-4 |
81-15-2 |
5-Tert-butyl-2,4,6-trinitro-m-xylene (1) |
NL |
Biodegradation simulation test for determination of half-life in marine environment |
18 months |
|
6 |
200-663-8 |
67-66-3 |
Chloroform (3) |
F |
Environmental exposure information for production and uses |
6 months |
|
Two long-term toxicity tests on sediment organisms |
6 months |
||||||
Toxicity tests on micro-organisms:
|
6 months |
||||||
7 |
202-974-4 |
101-77-9 |
4,4′-Methylenedianiline (2) |
D |
Long-term toxicity test on sediment organisms (Chironomus spec.) |
6 months |
|
Long-term toxicity test on sediment organisms (Hyalella azteca) |
6 months |
||||||
8 |
231-152-8 215-146-2 |
7440-43-9 1306-19-0 |
Cadmium (1) Cadmium oxide (1) |
B |
Ecotoxicity tests under very low water hardness conditions |
12 months |
|
Validation of applicability of SEM/AVS concept (bioavailability in sediment compartment) |
12 months |
||||||
9 |
231-668-3 |
7681-52-9 |
Sodium hypochlorite (3) |
IT |
Whole effluent assessment |
9 months |
|
10 |
247-148-4 |
25637-99-4 |
Hexabromocyclododecane (3) |
S |
Biodegradation simulation test providing valid half-lives as well as identification of metabolites |
8 months |
|
11 |
201-236-9 |
79-94-7 |
Tetrabromobisphenol-A (4) |
UK |
Clarification of use pattern |
9 months |
|
Long term toxicity test with Chironomus riparius in sediment |
9 months |
||||||
Long term toxicity test with Chironomus riparius in water |
9 months |
||||||
Toxicity study with molluscs |
9 months |
||||||
Investigation of degradation to bisphenol-A in sediment |
9 months |
||||||
12 |
287-476-5 |
85535-84-8 |
Alkanes, C10-13, chloro (SCCPs) (2) |
UK |
Environmental exposure information on emissions |
3 months |
|
Biodegradation simulation test to determine half-life in the marine environment |
18 months |
(1) Substance listed in the Annex to Commission Regulation (EC) No 143/97 (OJ L 25, 28.1.1997, p. 13; priority list No 3).
(2) Substance listed in the Annex to Commission Regulation (EC) No 1179/94 (OJ L 131, 26.5.1994, p. 3; priority list No 1).
(3) Substance listed in the Annex to Commission Regulation (EC) No 2268/95 (OJ L 231, 28.9.1995, p. 18; priority list No 2).
(4) Substance listed in the Annex to Commission Regulation (EC) No 2364/2000 (OJ L 273, 26.10.2000, p. 5; priority list No 4).