ISO-IEC 17025:2017 Section 7 - Process Requirements and Section 8 - Management System Requirements

By participating in this 3-part series, attendees will have a much better appreciation of what is old and what is new and/or different, And you will learn what is risk and how do you address it?

Michael Brodsky
Michael Brodsky
Thursday, June 20, 2019
09:00 AM PDT | 12:00 PM EDT
60 Minutes

More Trainings by this Expert   Product Id : 502536

Price Details
$150 Live
$290 Corporate Live
$190 Recorded
$390 Corporate Recorded
Combo Offers
Live + Recorded
$289 $340 Live + Recorded
Corporate (Live + Recorded)
$599 $680 Corporate
(Live + Recorded)
Price Detail Options

Many laboratories have successfully developed and implemented a functional quality management system based on the requirements of ISO/IEC 17025:2005.

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. A new version of this standard was released on November 19, 2017.

Have the rules changed? What is new and/or different with 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: What are the changes to the technical and management requirements and how should these be addressed? This webinar will discuss the old as well as the new changes in the standard and their impact on your QMS.

This is the 3rd of 3 parts to address the new standard. It will provide you with an overview of the salient differences and similarities between the old and the new requirements.

What is risk and how do you address it? By participating in this 3-part series, attendees will have a much better appreciation of what is old and what is new and/or different.

Areas Covered in the Session:

  • Review of requests, tenders and contracts
  • Selection, verification and validation of methods
  • Sampling
  • Handling of customer items
  • Technical records
  • Evaluation of uncertainty of measurement
  • Validity of results
  • Reporting of results
  • Complaints
  • Management of nonconforming work
  • Control of data - information management
  • Risk Analysis. What must my lab do to comply

Who Will Benefit:
  • Laboratory Managers
  • QA Managers
  • QC Analysts
  • College Student/Graduates in Science Programs

Speaker Profile
Michael Brodskyhas been an Environmental Microbiologist for more than 41 years. He is a Past President of the Ontario Food Protection Association and AOAC International. He serves as 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 as a chapter editor on QA for the Compendium of Methods in Microbiology. He is also a lead auditor/assessor in microbiology for the Canadian Association for Laboratory Accreditation (CALA) and is a member of the Board of Directors.

Your Recently Viewed Webinars

Payment Methods

Contact Us

NetZealous LLC,
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539, USA.


  Refund Policy
  Fax: 302 288 6884