ISO/IEC 17025:2017 Update: The New Standard for Laboratory Competence

Duration: 75 Minutes
This course is a comprehensive review of the changes made to ISO/IEC 17025 during its recent revision. In this course, you will be guided through the impact to your existing ISO/IEC 17025 compliant system, as well as the necessary steps to ensure compliance to the new standard.
ISO 17025 Quality Management Systems
Instructor: Michael Brodsky
Product ID: 507671
Objectives of the Presentation
Many laboratories have successfully developed and implementing a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025:2005 but also meets their needs. Some are still struggling to get accredited and even those already accredited still have issues as evidenced by the number of non-conformances cited during the subsequent biannual audits.
  • Have the rules changed? Recall the differences between ISO/IEC 172025:2005 and the newly revised version, ISO/IEC 17025:2017
  • What are the new requirements of ISO/IEC 17015:2017?
  • Identify the new documents and records required by the standard
  • How does the new standard impact laboratories that are already accredited and how do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits?
  • Implement a quality documentation transition plan to ensure compliance with the newly revised standard
Why Should you Attend
ISO/IEC 17025:2005 is the international standard for the General requirements for the competence of testing and calibration laboratories and is in the process of being updated and revised. The new version is expected to be released sometime in 2017. What are the changes and how will they impact your current Quality Management System? Similarly, developing a QMS is a prerequisite for getting accredited. What are the new requirements that need to be addressed? This webinar will discuss the changes in the standard and their impact on your QMS.

Areas Covered
To address the changes in ISO/IEC 17025 and their impact on Quality Management Systems
  • Defining a QMS
  • Management Components of a QMS
  • New and revised Quality Management Requirements
  • Technical Components of a QMS
  • New and revised Technical Requirements
  • Method Selection, Validation and Verification
  • Ensuring analytical competency
  • Identifying adjustments to your existing ISO/IEC 17025:2005 Quality Documentation
Who will Benefit
  • Laboratory Managers
  • QA Managers
  • QC Analysts
  • College student/graduates in Science programs
  • Laboratories accredited to ISO/IEC 17025:2005
  • Laboratories seeking to become accredited to ISO/IEC 17025
$375
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  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
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  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Michael Brodsky has been an Environmental Microbiologist for more than 48 years. He has a post-graduate degree from the University of Toronto, School of Hygiene and Tropical Medicine. He has experience in both the public and private sectors in food safety. He is a Past President of the International Association for Food Protection, the Ontario Food Protection Association and AOAC International. He serves as co-Chair for the AOAC Expert Review Committee for Microbiology, as a scientific reviewer in Microbiology for the AOAC Official Methods of Analysis and the AOAC Research Institute. He is a reviewer for Standard Methods for the Examination of Water and Wastewater and a chapter co-editor on QA for the Compendium of Methods in Microbiology. He is also a technical assessor in microbiology for the Standard Council of Canada and a lead auditor/assessor for the Canadian Association for Laboratory Accreditation.
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