1. Article
5, Article
6, Article
7(1), Article
17, Article
18 and Article
21 shall not apply until 1 December 2010 to the following
substances:
(a)
phase-in substances classified as carcinogenic,
mutagenic or
toxic to reproduction, category 1 or 2, in accordance with Directive 67/548/EEC and manufactured in the Community or imported,
in quantities reaching one tonne or more per year per manufacturer or per
importer, at least once after 1 June 2007;
(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;
(c)
phase-in substances manufactured in the Community or imported, in quantities reaching 1000 tonnes or more per year per manufacturer or per
importer, at least once after 1 June 2007.
2. Article
5, Article
6, Article
7(1), Article
17, Article
18 and Article
21 shall not apply until 1 June 2013 to
phase-in substances 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.
3. Article
5, Article
6, Article
7(1), Article
17, Article
18 and Article
21 shall not apply until 1 June 2018 to
phase-in substances manufactured in the Community or imported, in quantities reaching one tonne or more per year per manufacturer or per
importer, at least once after 1 June 2007.
4. Without prejudice to paragraphs 1 to 3, a
registration can be submitted at any time before the relevant deadline.