Quality Management Program - Laboratory Services

   

QMP-LS Home Ontario Laboratory Accreditation (OLA)

 

About OLA 

Background and Operating Principles

Development of OLA began on September 15, 2000. OLA was implemented in 2003.

Accreditation services are provided to licensed Ontario medical laboratories under agreement with the MOHLTC, and laboratories from other jurisdictions in Canada or other countries may voluntarily apply for accreditation. Applicant laboratories for voluntary accreditation are assessed by QMP–LS and issued ISO 15189 certificates by the Standards Council of Canada (SCC) under a partnership agreement (see “Partnership with Standards Council of Canada”).

Operations comply with the following international standard and guidelines:

  • ISO/IEC 17011:2004 Conformity assessment–General requirements for accreditation bodies accrediting conformity assessment bodies

  • ILAC-G11:07/2006 ILAC Guidelines on Qualification and Competence of Assessors and Technical Experts

  • ILAC-G3:1994 ILAC Guidelines for Training Courses for Assessors Used by Laboratory Accreditation Schemes

This standard, guidelines and the resulting operating principles distinguish the OLA medical laboratory accreditation program from others available in North America in the following ways:

  • Volunteer assessors are pre-certified through a comprehensive assessor training program, consisting of 18 hours of self-study, 2½ days of classroom training, formal examination and annual refreshers to maintain certification.

  • All OLA accreditation assessment teams are accompanied on site by a QMP–LS staff technologist. This ensures consistency in the assessment process, that impartiality is maintained, and that confidentiality is observed. Assessment teams contain technical experts in all areas covered under the scope of accreditation.

  • Key assessor competencies form the basis of performance evaluations.

  • A QMP–LS quality management system facilitates consistency in processes, identification of non-conformities, corrective and preventive actions, complete and controlled documentation and records, and integration with the EQA division for ongoing surveillance in accredited laboratories.

  • Certificates to ISO 15189 are issued by SCC (conditions apply – see “Agreement with Standards Council of Canada”).

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Revised: 2008-10-03


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