ISO/ IEC 17025:2017 Update: Everything Old is New Again


Michael Brodsky, Keynote Speaker at Compliance Key INC. He has been an Environmental Microbiologist for more than 42 years. He is a Past President of the Ontario Food Protection Association (OFPA), the International Association for Food Protection (IAFP) 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 OMA and the AOAC Research Institute, as a reviewer for Standard Method for the Examination of Water and Wastewater ....

Overview

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? What are the new requirements of ISO/IEC 17015:2017? 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?

Why should you attend this webinar?

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 what you must do to update your QMS to meet the new requirements.

Areas Covered in the Session:

  • Changes in ISO/IEC 17025 and their impact on Quality Management Systems
  • Defining a QMS
  • Management Components of a QMS
  • Technical Components of a QMS
  • Method Selection, Validation and Verification
  • Ensuring analytical competency

Who can Benefit:

  • Laboratories accredited to ISO/IEC 17025:2005
  • Laboratories seeking to become accredited to ISO/IEC 17025.



Webinar Id: LSHCMBI003

Training Options:

Duration: 60 mins

 07/03/2017

 10:00 AM PST | 01:00 PM EST

 Single Attendee: [Only for one participant]

 $179 (Live)                    $304 (Live + Recorded)

 Multiple Attendee: [For a group of 2-5 participants]

 $363 (Live)                    $488 (Live + Recorded)

 Corporate Attendee: [For a group of 6-10 Participants]

 $726 (Live)                    $945 (Live + Recorded)

 Recorded: [Six month unlimited access]

 $217(Single Attendee)  $599 (Unlimited Attendee)

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