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  • ISO/IEC 17020:2012 Inspection Agencies
  • ISO/IEC 17021-1:2015 Management System CBs
  • Advanced IAF Mandatory Document Course
  • ISO/IEC 17024:2012 Personnel Certification Bodies
  • ISO/IEC 17025:2017 for Testing and Calibration Labs
  • ISO 17034 Reference Material Producer (RMP) Course
  • ISO IEC 17043 Proficiency Testing Provider (PTP) Course
  • The NELAC Institute (TNI) Environmental Lab Accreditation Training
    • TNI 90 Minute Webinars
  • ISO 15189:2012 Understanding the Requirements
  • ISO/IEC 17065:2012 Product Certification Agencies
  • Uncertainty of Measurement
  • Understanding Risk Approach for Management Systems
  • Internal Audit Course for Clinical/Medical Laboratories under 15189
  • Lead Assessor Course
  • Internal Audit Course for All Standards
  • Root Cause Analysis and Corrective Action Course
  • Special Inspection Agencies (SIA) in Building Construction – NYC Focus
  • Building Department Accreditation #101 Using AC251
  • Fire Prevention Department Accreditation #101 Using AC426
  • Managing the IAS AC172 Fabricator Inspection Programs for Structural Steel Requirements
  • Managing the IAS AC472 Metal Building Systems Accreditation Requirements
  • Managing the IAS AC473 Metal Building Systems Accreditation Requirements
  • Managing Combined IAS Structural Steel and Metal Building Inspection Programs AC172, AC472 and AC473 Requirements
  • AC478 Inspection Practices of Metal Building Assemblers In Simple Language

ISO 15189:2012 Understanding the Requirements

ISO 15189 for Medical/Clinical Laboratories.

Understanding ISO 15189

Understand and interpret the requirements of ISO 15189, including its QMS. Identify required documents and understand a risk management plan.

Complete Overview
Receive a complete overview of ISO 15189 with valuable insights and tools to help you implement the requirements of the standard. See the detailed Course Outline/Syllabus here.

Learn Key Applications in the Standard: Who Should Attend?
  • Internal Audits & Management Reviews
  • Clinical Testing Criteria
  • Complaint Handling Processes
  • Corrective Actions and Preventative Actions
  • Training
  • Confidence Region for Clinical Results
  • Traceability of Measurement
  • Pathologists,
  • Clinical Microbiologists,
  • Clinical Biochemists and Technicians
  • Those working in Medical labs with a need to understand ISO 15189
  • Consultants

This training will help you understand the key concepts in ISO 15189 for implementing a quality management system, a prerequisite for clinical laboratory accreditation.

DATE(S) AND LOCATION(S):

See https://www.iasonline.org/training/ias-training-schedule/

EARLY REGISTRATION*

$900.00 USD (Outside of US and Canada)
$700.00 USD (US and Canada only)
$500.USD (India only)
$350.USD (Webinar only)

REGULAR REGISTRATION*

$1,100.00 USD (Outside of US and Canada)
$900.00 USD (US and Canada only)
$650.USD (India only)
$400.USD (Webinar only)

*  Early registration cut-off is normally 21 days prior to the scheduled training event.

5% additional discount for 2nd, 3rd, or more students from the same company attending the same training course. Space is Limited to 20 people for each training session.

Fees are non-refundable for cancellations; however, you may substitute another member of your staff, or attend another class offered by IAS at a later date.  If IAS cancels this class for any reason, the full registration fee paid will be refunded.

Request Additional Information  Contact Ms. Jouliana Tchiloyans at jtchiloyans@iasonline.org.

Request and Pay for Training Here

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