Registration Dossier

Diss Factsheets

Administrative data

Endpoint:
repeated dose toxicity: oral
Study period:
May 22, 2007 - September 26, 2007
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Study conform to Directive 96/54/EC, B.7 and OECD Guideline No. 407
Data waiving:
other justification
Justification for data waiving:
other:

Data source

Materials and methods

Test material

Results and discussion

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion