Registration Dossier

Administrative data

Endpoint:
eye irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Guideline study-GLP compliance

Data source

Reference
Reference Type:
other:
Title:
Unnamed
Year:
2011

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
other: ANNEX V, B.5
GLP compliance:
yes

Test material

Reference
Name:
Unnamed
Type:
Constituent

Results and discussion

In vivo

Results
Remarks on result:
other: Not provided in information from migrated NONS file, as per inquiry number 06-0000020885-62-0000, permission to refer granted by ECHA.

Applicant's summary and conclusion