Registration Dossier

Toxicological information

Skin sensitisation

Currently viewing:

Administrative data

Endpoint:
skin sensitisation: in vivo (LLNA)
Type of information:
other: Testing proposal
Adequacy of study:
other information
Rationale for reliability incl. deficiencies:
guideline study
Justification for type of information:
The OECD reccommended in vitro test is not capable of differentiating between a Cat 1 and a Cat 2 sensitiser. As the substance is likely sensitising, an in vivo LLNA should be conducted to ensure robust data on the substance. Approval is needed from ECHA to conduct an in vivo LLNA, in the mean time classification as sensitising has been accepted.

Data source

Materials and methods

Results and discussion

Applicant's summary and conclusion