Registration Dossier

Diss Factsheets

Administrative data

Endpoint:
skin sensitisation, other
Remarks:
Will be tested in QSAR
Type of information:
(Q)SAR
Adequacy of study:
weight of evidence
Reliability:
other: Will be tested in QSAR
Justification for type of information:
QSAR studie will be done ba Covance in UK.We have been in contact with ECHA, VU501539-02 communication number SUB-C-2114443145 -56 -01/F.
No operators have direct contact with the product.
There are no other registrants of this substance.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2019
Report date:
2018

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: QSAR planned
Principles of method if other than guideline:
QSAR
GLP compliance:
not specified
Remarks:
QSAR test will be done

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
solid: bulk
Details on test material:
Iodixanol reference standard (Nycomed J.no. 795/185-1 (12))

Results and discussion

In vivo (LLNA)

Results
Parameter:
other: QSAR planned
Remarks on result:
not measured/tested

Applicant's summary and conclusion

Executive summary:

QSAR studie will be done ba Covance in UK.We have been in contact with ECHA, VU501539-02 communication number SUB-C-2114443145 -56 -01/F.

No operators have direct contact with the product.

There are no other registrants of this substance.