ISO 15189:2022 Understanding the Requirements
ISO 15189 for Medical/Clinical Laboratories including Point-of-Care Testing (POCT)
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? | |
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This training will help you understand the key concepts in ISO 15189 for implementing a quality management system, a prerequisite for clinical laboratory accreditation.
FREE WEBINARS ON 15189
New for 2024 – Live 2 hour Webinar on 7 March 2024
This Webinar will introduce the revised ISO 15189:2022 with highlights on the new requirements
different from the previous version of ISO 15189:2012. This will help medical laboratories to address
the gaps between previous and new versions of ISO 15189 and transfer their existing management
systems to the new version per ILAC & IAS transitional requirements.
Time
10:00 am -12:00 pm (Saudi Time)
Who should attend
Medical Professionals involved in medical testing and point-of-care testing,
Owners/management personnel of Medical Laboratories, Consultants, Quality Personnel, Assessors,
Regulators, and Internal Auditors
See https://www.iasonline.org/training/ias-training-schedule/
Previous Webinars
Click on any of the numbered webinar links below to see the course description for that webinar. Following each webinar, IAS creates a video of the webinar and posts it to our online training site at https://international-accreditation-service.teachable.com/courses/category/iso-15189-module
| Module 1 - Resources and Infrastructure | 21 April 2021 |
| Module 2 - Methods and Processes | 21 May 2021 |
| Module 3 - Process Management and Outcomes | 22 June 2021 |
| Module 4 - System Management Policies | 20 July 2021 |
| Module 5 - Control of Records | 17 August 2021 |
| Module 6 - QA and QC | 22 September 2021 |
| Module 7 - Auditing the Lab | 12 October 2021 |
| Module 8 - Traceability of Measurement | 16 November 2021 |
DATE(S) AND LOCATION(S):
See https://www.iasonline.org/training/ias-training-schedule/
EARLY REGISTRATION*
$950.00 USD (Outside of US and Canada)
$750.00 USD (US and Canada only)
$500.00 USD (India only)
$450.00 USD (Webinar only)
REGULAR REGISTRATION*
$1,200.00 USD (Outside of US and Canada)
$950.00 USD (US and Canada only)
$650.00 USD (India only)
$500.00 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.
