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REACH - Registration, Evaluation and Authorisation of Chemicals
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REACH - Registration, Evaluation and Authorisation of Chemicals
TITLE-II
: REGISTRATION OF SUBSTANCES
CHAPTER-4
: Common provisions for all registrations
ARTICLE 22
: Further
duties
of
registrants
ARTICLE 22:
Further
duties
of
registrants
1. Following
registration
, a
registrant
shall be
responsible
on his own
initiative
for updating his
registration
without undue
delay
with
relevant
new
information
and submitting it to the
Agency
in the following
cases
:
(a) any
change
in his
status
, such as being a
manufacturer
, an
importer
or a
producer
of
articles
, or in his
identity
, such as his
name
or
address
;
(b) any
change
in the composition of the
substance
as given in section 2 of Annex VI;
(c)
changes
in the
annual
or total
quantities
manufactured
or imported by him or in the
quantities
of
substances
present in
articles
produced or imported by him if these result in a
change
of
tonnage
band
,
including
cessation
of
manufacture
or
import
;
(d) new
identified uses
and new uses advised against as in section 3.7 of Annex VI for which the
substance
is
manufactured
or imported;
(e) new
knowledge
of the
risks
of the
substance
to
human health
and/or the
environment
of which he may reasonably be expected to have become aware which
leads
to
changes
in the
safety
data
sheet or the
chemical
safety
report
; (f) any
change
in the
classification
and
labelling
of the
substance
;
(g) any update or
amendment
of the
chemical
safety
report
or section 5 of Annex VI;
(h) the
registrant
identifies
the need to perform a
test
listed in Annex IX or Annex X, in which
cases
a
testing
proposal
shall be developed;
(i) any
change
in the
access
granted
to
information
in the
registration
.
The
Agency
shall
communicate
this
information
to the
competent authority
of the
relevant
Member State
.
2. A
registrant
shall submit to the
Agency
an update of the
registration
containing the
information
required by the
decision
made in
accordance
with
Articles
40
,
41
or
46
or take into
account
a
decision
made in
accordance
with
Articles
60
and
73
, within the deadline specified in that
decision
. The
Agency
shall notify the
competent authority
of the
relevant
Member State
that the
information
is available on its database.
3. The
Agency
shall
undertake
a completeness check according to
Article
20
(2) first and second subparagraphs of each updated
registration
. In
cases
where the update is in
accordance
with
Article
12
(2) and with paragraph 1(c) of this
Article
then the
Agency
shall check the completeness of the
information
supplied by the
registrant
and
Article
20
(2) shall apply adapted as necessary.
4. In
cases
covered by
Articles
11
or
19
, each
registrant
shall submit separately the
information
specified in paragraph 1(c) of this
Article
.
5. An update shall be accompanied by the
relevant
part of the
fee
required in
accordance
with Title IX.
[
Next page
]
Referred by:
ARTICLE 16
:
Duties
of the
Commission
, the
Agency
and
registrants
of
substances
regarded as being
registered
ARTICLE 20
:
Duties
of the
Agency
ARTICLE 21
:
Manufacturing
and
import
of
substances
ARTICLE 37
:
Downstream user
chemical
safety
assessments
and
duty
to
identify
, apply and recommend
risk
reduction
measures
ARTICLE 74
:
Fees
and
charges