Registration Dossier

Diss Factsheets

Administrative data

Endpoint:
acute toxicity: oral
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 test is conducted by means of Read Across approach. Further information was attached at section 13

Data source

Reference
Reference Type:
other: other company data
Title:
Unnamed
Year:
2018

Materials and methods

Principles of method if other than guideline:
Test method under evaluation
GLP compliance:
yes (incl. QA statement)
Test type:
other: test in progress

Test material

Constituent 1
Reference substance name:
Similar Substance 02 - AO061:1
IUPAC Name:
Similar Substance 02 - AO061:1
Test material form:
solid: particulate/powder

Administration / exposure

Route of administration:
oral: unspecified

Results and discussion

Effect levels
Remarks on result:
other: test in progress

Applicant's summary and conclusion

Conclusions:
Test in progress.