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HTLV Serology

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The National Laboratory for HIV Reference Services is accredited to ISO/IEC 17043 by the Standards Council of Canada for the specific scopes of accreditation published on www.scc.ca.

The NLHRS will be temporarily pausing its Quality Assessment Program for the upcoming October 2024 and April 2025 testing events.  During this pause, we will not be sending out proficiency testing panels for HTLV serology.

Details

Pathogen:
Human T-lymphotropic virus (HTLV)
Laboratory:
National Laboratory for HIV Reference Services
Phone #:
(204) 789-6522
Fax:
(204) 318-2221
Email:
Frequency:
2 test events per year, shipped once per year in October.
Description:

Proficiency panel for the detection of HTLV-I and HTLV-II antibodies.

Scope:

The NLHRS HTLV Serology Quality Assurance Program was established in 1997 to monitor HTLV Serology testing in Canadian and international labs. The participants are asked to follow their testing algorithm to identify the presence of HTLV-I and HTLV-II antibodies.

Fees:

There is no cost to the participants. Shipping fees may be applied for participants who routinely do not return results.

Eligibility criteria for participation:

This program is open to any Canadian lab that performs HTLV Serology testing. For international labs, there may be a restriction due to shipping/cost requirements.   Participants may be suspended or shipping costs may be applied if a lab does not return results.

NML Transfer permit:

The NLHRS is required to obtain a permit for sending the proficiency panel to our participants. The QAP coordinator will provide Form SES-F-052A to the participants for them to complete and return with the required documentation to the QAP coordinator. 

The transfer permit has an expiry date; the QAP coordinator will contact the participants to initiate the process for renewal of the transfer permit. 

 

Confidentiality arrangements:

Confidentiality, collusion, and falsification of data policy:

Participants are randomly assigned alpha-numeric identifiers that allow labs and their information to remain confidential.  If an interested party requires the proficiency testing results to be directly provided by the proficiency testing provider, the participants shall be made aware of the arrangement in advance of participation.  In exceptional circumstances, when a regulatory authority requires proficiency testing results to be directly provided to the authority by the proficiency testing provider, the affected participants shall be notified of this action in writing.

The NLHRS has a zero tolerance policy for collusion and falsification of proficiency testing results. Participants suspected of breaching this policy will be investigated by the NLHRS, which may result in suspension or removal from the proficiency testing program.

 

How to apply:

Submit your request to nlhrs.qap-peq.lnsrv@phac-aspc.gc.ca.

Appeal process:

Participants have the right to appeal the results of any proficiency test (PT) in which they are enrolled.

Any appeals received will be acknowledged, validated, and investigated, with the outcome communicated to the participant.

If you would like to make an appeal on your results found in the QAP report, please submit your request to nlhrs.qap-peq.lnsrv@phac-aspc.gc.ca.

Reports

HTLV Serology Quality Assessment Program Final Report Oct 2018
2018Oct26 HTLV serology Final Report 2019-01-16.pdf

HTLV Serology Quality Assessment Program Final Report Oct 2015
2015Oct22 HTLV.Final Report.pdf

HTLV Serology Quality Assessment Program Final Report Oct 2016
2016Oct28 HTLV Serology Final Report 18-Jan-17.pdf

HTLV Serology Quality Assessment Program Final Report Apr 2017
2017Apr19 HTLV serology Final Report 2017-06-27.pdf

Revised HTLV Serology Quality Assessment Program Final Report Oct 2017
Revised 2017Oct27 HTLV Final Report 2018-01-22.pdf

HTLV Serology Quality Assessment Program Final Report Apr 2019
2019Apr16 HTLV serology Final Report 2019-08-02.pdf

HTLV Serology Quality Assessment Program Final Report Apr 2016
2016Apr21 HTLVSER.Final Report 2016-06-07.pdf

HTLV Serology Quality Assessment Program Final Report Apr 2018
2018Apr19 HTLV serology Final Report Aug-15-18.pdf

HTLV Serology Quality Assessment Program Final Report Oct 2019
2019Oct31 HTLV Serology Final Report 2019-12-23.pdf

HTLV Serology Quality Assessment Program Final Report Apr 2021
2021Apr19 HTLV serology Final Report July 19, 2021.pdf

HTLV Serology Quality Assessment Program Final Report Oct 2020
2020Oct30 HTLV Serology Final Report 2021-03-05.pdf

HTLV Serology Quality Assessment Program Final Report Apr 2024
2024Apr16 HTLV Serology Final Report 2024-07-15.pdf

HTLV Serology Quality Assessment Program Final Report Oct 2023
2023Oct31 HTLV Serology Final Report 2024-01-29.pdf

HTLV Serology Quality Assessment Program Final Report Nov 2022
2022Nov14 HTLV Serology Final Report 2023-02-07.pdf

Revised - HTLV Serology Quality Assessment Program Final Report Apr 2021
Revised 2021Apr19 HTLV serology Final Report 2021-08-13.pdf

HTLV Serology Quality Assessment Program Final Report Oct 2021
2021Oct29 HTLV serology Final Report 2021-12-02.pdf

HTLV Serology Quality Assessment Program Final Report Apr 2022
2022Apr19 HTLV Serology Final Report 2022-07-14.pdf

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