ComplianceOnline

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

Instructor: Michael Brodsky
Product ID: 705272
  • Duration: 60 Min
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This training program will discuss in details the new requirements of ISO/IEC 17015:2017 laboratory accreditation standard and their impact on quality management system. Learn best practices to ensure compliance to minimize corrective actions arising from accreditation audits.

Why Should You Attend:

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?

This webinar will discuss the changes in the standard and their impact on your QMS.

Areas Covered in the Webinar:

  • Defining a QMS
  • Management Components of a QMS
  • Technical Components of a QMS
  • Method Selection, Validation and Verification
  • Ensuring Analytical Competency

Who Will Benefit:

  • Laboratory Managers
  • QA Managers
  • QC Analysts
  • Analytical Support Personnel
  • Laboratory Quality Management Staff
Instructor Profile:
Michael Brodsky

Michael Brodsky
Lead Auditor, Canadian Association for Laboratory Accreditation

Michael Brodsky has been an Environmental Microbiologist for more than 44 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 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 editor on QA for the Compendium of Methods in Microbiology.

Michael is also a technical assessor in microbiology for the Standards Council of Canada (SCC) and a lead auditor/assessor for the Canadian Association for Laboratory Accreditation (CALA).

Topic Background:

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?

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

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