Registration Dossier

Administrative data

Endpoint:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Studies with regard to acute oral toxicity via other routes, acceptable for assessment, also peer-reviewed under Regulation 793/93.

Data source

Reference
Reference Type:
other: EU Risk Assessment Report (RAR)
Title:
Trichloroethylene
Author:
Rapporteur: United Kingdom, on behalf of the European Union
Year:
2004

Materials and methods

Principles of method if other than guideline:
Acute Toxicicity: Other routes (intraperitoneal route and various other routes of exposure)

Test material

Reference
Name:
Unnamed
Type:
Constituent
Type:
Constituent

Administration / exposure

Route of administration:
intraperitoneal

Results and discussion

Effect levels
Remarks on result:
other: None of the study was considered to provide any additional information useful for hazard identification or human health risk assessment.

Applicant's summary and conclusion