• Sample Details 10mg freeze-dried sample in glass vials. A panel of simulated bovine samples are representative of tissue, faeces, fluid and swabs containing varying concentrations of a non–toxigenic strain of E. coli O157 and contaminants.
  • Method Culture and identification

Overview

The purpose of the scheme is for participants to demonstrate they are able to isolate and identify the presence of the E.coli O157 (non- toxogenic strain).

Result input

Results are returned through our electronic reporting system.

ID: Result (Positive / Negative / Inconclusive)

Results deadline (from date of shipping)

21 days

PT Report

Authorised report will be published electronically. These will show intended result and results from all participants

Accreditation Status

ISO/IEC 17043 Conformity assessment – General requirements for proficiency testing.

Health and Safety

This material is for in vitro use only, not for use in animals.

Import Permit

It is the responsibility of the participants to check with their customs authority if an import permit is required to import VETQAS® PT samples. If a permit is required, we must receive a valid copy of the permit before the scheduled distribution date. Please note, if we do not receive the permit by the scheduled distribution date the samples will not be shipped and there will be no refund.

Provision of external services

Aspects of the Proficiency Testing schemes may at times be performed by a competent external service provider, for which VETQAS® is responsible.