- Latest available (Revised)
- Original (As adopted by EU)
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)
When the UK left the EU, legislation.gov.uk published EU legislation that had been published by the EU up to IP completion day (31 December 2020 11.00 p.m.). On legislation.gov.uk, these items of legislation are kept up-to-date with any amendments made by the UK since then.
Legislation.gov.uk publishes the UK version. EUR-Lex publishes the EU version. The EU Exit Web Archive holds a snapshot of EUR-Lex’s version from IP completion day (31 December 2020 11.00 p.m.).
This version of this Regulation was derived from EUR-Lex on IP completion day (31 December 2020 11:00 p.m.). It has not been amended by the UK since then. Find out more about legislation originating from the EU as published on legislation.gov.uk.![]()
Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.
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:
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.
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
| a Substance listed in the Annex to Commission Regulation (EC) No 143/97 (OJ L 25, 28.1.1997, p. 13; priority list No 3). | ||||||
| b Substance listed in the Annex to Commission Regulation (EC) No 1179/94 (OJ L 131, 26.5.1994, p. 3; priority list No 1). | ||||||
| c Substance listed in the Annex to Commission Regulation (EC) No 2268/95 (OJ L 231, 28.9.1995, p. 18; priority list No 2). | ||||||
| d Substance listed in the Annex to Commission Regulation (EC) No 2364/2000 (OJ L 273, 26.10.2000, p. 5; priority list No 4). | ||||||
| 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′-Isopropylidenediphenola | 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 acetateb | 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-Furaldehydec | 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 phthalatea | 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-xylenea | NL | Biodegradation simulation test for determination of half-life in marine environment | 18 months |
| 6 | 200-663-8 | 67-66-3 | Chloroformc | 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′-Methylenedianilineb | 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 | Cadmiuma Cadmium oxidea | 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 hypochloritec | IT | Whole effluent assessment | 9 months |
| 10 | 247-148-4 | 25637-99-4 | Hexabromocyclododecanec | S | Biodegradation simulation test providing valid half-lives as well as identification of metabolites | 8 months |
| 11 | 201-236-9 | 79-94-7 | Tetrabromobisphenol-Ad | 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)b | UK | Environmental exposure information on emissions | 3 months |
| Biodegradation simulation test to determine half-life in the marine environment | 18 months | |||||
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).
Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.
Original (As adopted by EU): The original version of the legislation as it stood when it was first adopted in the EU. No changes have been applied to the text.
Geographical Extent: Indicates the geographical area that this provision applies to. For further information see ‘Frequently Asked Questions’.
Show Timeline of Changes: See how this legislation has or could change over time. Turning this feature on will show extra navigation options to go to these specific points in time. Return to the latest available version by using the controls above in the What Version box.
Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:
This timeline shows the different versions taken from EUR-Lex before exit day and during the implementation period as well as any subsequent versions created after the implementation period as a result of changes made by UK legislation.
The dates for the EU versions are taken from the document dates on EUR-Lex and may not always coincide with when the changes came into force for the document.
For any versions created after the implementation period as a result of changes made by UK legislation the date will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. For further information see our guide to revised legislation on Understanding Legislation.
Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:
Click 'View More' or select 'More Resources' tab for additional information including: