Registration Dossier

Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Type of information:
other: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
test procedure in accordance with national standard methods with acceptable restrictions
Remarks:
The reliability of the read-across experimental study is established to be R2. Justification for readacross is detailed at section 13.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2018

Materials and methods

Principles of method if other than guideline:
Test method under evaluation
GLP compliance:
yes (incl. certificate)
Type of assay:
other: Test method under evaluation

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
solid: particulate/powder

Results and discussion

Test results
Species / strain:
other: test in progress
Metabolic activation:
not applicable
Genotoxicity:
other: test in progress
Cytotoxicity / choice of top concentrations:
other: test in progress
Remarks on result:
other: test in progress

Applicant's summary and conclusion

Conclusions:
Test in progress.