Registration Dossier

Toxicological information

Specific investigations: other studies

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Administrative data

Endpoint:
specific investigations: other studies
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Studies were perforemd according to US EPA guidelines.

Data source

Materials and methods

Results and discussion

Applicant's summary and conclusion

Conclusions:
According to the final decision of ECHA in 2015 study reports of endocrine assays submitted under the Endocrine Disruptor Screening Program have to be submitted. All in vitro reports are attached under this endpoint record.