PJLA Webinars

PJLA is now offering free webinars on various topics for both testing and calibration laboratories. These are for all interested parties including: laboratories seeking accreditation, accredited laboratories, assessors and consultants.

Free Webinars

PJLA FREE WebinarsPJLA is now offering free webinars on various topics in relation to ISO/IEC 17025:2005 for both testing and calibration laboratories.
These are for all interested parties including: laboratories seeking accreditation, accredited laboratories, assessors and consultants.

Upcoming Webinars:


1pm EST Tuesday, May 22
Section 7.8.6 Reporting Statements of Conformity to Include the Decision Rule Requirements Specified in ISO/IEC 17025:2017

Participants will be educated on the requirements of ISO/IEC 17025:2017, Section 7.8.6, Reporting Statements of Conformity in relation to Decision Rules. This will include an overview of the documentation requirements and the required associated risks that may be applied to this process.

Who Should Attend?
– Current Accredited Laboratories
– Laboratories Seeking Accreditation
– Regulators or Specifiers
– Assessors and Consultants

Click here to register!


1pm EST Thursday, June 28
ISO/IEC 17025:2017 A Look at Section 8.5 – Actions to Address Risks and Opportunities – Including Tools that can be Utilized by Organizations to Comply with this Section

Participants will be educated on the requirements of ISO/IEC 17025:2017, Section 8.5, Actions to Address Risks and Opportunities including the process for identifying risks, the development of preventive tools to reduce or eliminate risks and the evaluation of the effectiveness of the related actions.

Who Should Attend?
– Current Accredited Laboratories
– Laboratories Seeking Accreditation
– Regulators or Specifiers
– Assessors and Consultants

Click here to register!


1pm EST Thursday, July 26
A look at the ISO/IEC 17025:2017 Requirements Concerning Document Control and Control of Records

ISO/IEC 17025:2017 requires laboratories to control all documents, which include both internal and external documents. Control of records are now broken into technical and quality related records, and these new requirements are less prescriptive which allows laboratories more flexibility than what was originally stated in the 2005 Standard. The webinar will review the requirements specified in Sections 7.5 and 8.4 as presented in the 2017 Standard.

Who Should Attend?
– Current Accredited Laboratories
– Laboratories Seeking Accreditation
– Regulators or Specifiers
– Assessors and Consultants

Click here to register!


1pm EST Thursday, August 23
Option A and B as presented in ISO/IEC 17025:2017 Along with the Management System Documentation (8.2)

In this webinar, the concept of Option A vs. Option B as it relates to ISO/IEC 17025:2017 will be discussed, as well as explaining how both options have the same end results. Since there is no requirement for a Quality Manual, the 2017 Standard is more up to date with today’s technology. This webinar will analyze these advances, along with other significant changes that were required in the 2005 Standard but are not included in the 2017 Standard.

Who Should Attend?
– Current Accredited Laboratories
– Laboratories Seeking Accreditation
– Regulators or Specifiers
– Assessors and Consultants

Click here to register!


1pm EST Thursday, September 27
Section 7.8 of ISO/IEC 17025:2017 Reporting of Results

This webinar will look at the requirements specified in Section 7.8 of ISO/IEC 17025:2017. This includes both common and specific requirements for testing, calibration, and sampling. A new section has been added in regards to reporting statements of conformity. Details will be provided to help organizations comply with these new requirements.

Who Should Attend?
– Current Accredited Laboratories
– Laboratories Seeking Accreditation
– Regulators or Specifiers
– Assessors and Consultants

Click here to register!



Click to View Past Webinars