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REACH - Registration, Evaluation and Authorisation of Chemicals
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quantitative
[
Global Index
]
PREAMBLE
[
go to this PREAMBLE
]
... 38. The
generation
of
information
by alternative means
offering
equivalence
to prescribed
tests
and
test
methods
should also be allowed, for example when this
information
comes from
valid
qualitative or
quantitative
structure
activity
models
or from structurally related
substances
. To this end the
Agency
, in
cooperation
with
Member States
and interested
parties
, should develop appropriate
guidance
. It should also be possible not to submit certain
information
if appropriate justification can be provided. Based on
experience
gained through RIPs,
criteria
should be developed defining what constitutes such justification. ...
ARTICLE-13
: General requirements for generation of information on intrinsic properties of substances [
go to this ARTICLE
]
... 1.
Information
on intrinsic properties of
substances
may be generated by means other than
tests
, provided that the
conditions
set out in Annex XI are met. In particular for
human
toxicity
,
information
shall be generated whenever possible by means other than
vertebrate animal
tests
, through the use of alternative
methods
, for example,
in vitro
methods
or qualitative or
quantitative
structure
-
activity
relationship
models
or from
information
from structurally related
substances
(grouping or
read
-across).
Testing
in
accordance
with Annex VIII, section 8.6 and 8.7, Annex IX and Annex X may be omitted where justified by
information
on
exposure
and
implemented
risk management
measures
as specified in Annex XI, section 3. ...
ARTICLE-138
: Review [
go to this ARTICLE
]
... 3. The
report
, referred to in
Article
117
(4), on the
experience
acquired with the
operation
of this
Regulation
shall
include
a
review
of the
requirements
relating to
registration
of
substances
manufactured
or imported only in
quantities
starting at 1 tonne but less than 10 tonnes per
year
per
manufacturer
or
importer
. On the basis of that
review
, the
Commission
may present
legislative
proposals
to modify the
information
requirements
for
substances
manufactured
or imported in
quantities
of 1 tonne or more up to 10 tonnes per
year
per
manufacturer
or
importer
, taking into
account
the latest
developments
, for example in
relation
to alternative
testing
and (
quantitative
)
structure
-
activity
relationships ((Q)SARs). ...
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