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REACH - Registration, Evaluation and Authorisation of Chemicals
TITLE-II
: REGISTRATION OF SUBSTANCES
CHAPTER-5
: Transitional provisions applicable to phase-in substances and notified substances
ARTICLE 23
:
Specific provisions
for
phase-in substances
ARTICLE 23:
Specific provisions
for
phase-in substances
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 1 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 1 000 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 1 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.
5. This
Article
shall also apply to
substances
registered
under
Article
7
adapted as necessary.
[
Next page
]
Referred by:
ARTICLE 5
: No
data
, no
market
ARTICLE 20
:
Duties
of the
Agency
ARTICLE 21
:
Manufacturing
and
import
of
substances
ARTICLE 28
:
Duty
to pre-
register
for
phase-in substances
ARTICLE 29
:
Substance Information Exchange Fora
ARTICLE 37
:
Downstream user
chemical
safety
assessments
and
duty
to
identify
, apply and recommend
risk
reduction
measures