The PJLA Podcast

ISO/IEC 17025 Section 7.6 - Evaluation of Measurement Uncertainty

Presented by PJLA's Michael Kramer

 

Common Findings Detected on Environmental Lab Assessments

This webinar will educate participants on top common findings detected during environmental laboratory assessments including assessments to the DOD ELAP, DOECAP and TNI EL standards. Additionally, an overview of PJLA’s accreditation program requirements will be provided to educate participants on what to expect prior to the on-site assessment, corrective action timelines, report submissions including requirements of state program reporting.

A Look at ISO/IEC 17025:2017 - Section 7.7 & Associated Requirements Within PL-1

ISO/IEC 17025:2017 - Section 7.7 & associated requirements within PL-1 “PJLA Policy on Proficiency Testing” The requirements in section 7.7 of ISO/IEC 17025:2017 will be reviewed. This includes activities associated with internal control and well as comparison to sources outside your organization. We will look at the requirements specified in PJLA PL-1 regarding proficiency testing which would include developing an approved four year proficiency testing plan along with approved means of proficiency testing. Presented By: Michael Kramer, PJLA Calibration Program Manager and Lead Assessor

Improve Your Force Measurements: Tips to Improve Your Force Measurements

Presented by Perry Johnson Laboratory Accreditation

A Look at ISO/IEC 17025:2017 - Section 7.8 “Reporting of Results”

Presented by Michael Kramer of Perry Johnson Laboratory Accreditation

The Metals in Cannabis Method with first action status by AOAC & The Road to Get There…

In this webinar, we cover our new AOAC metals in the Cannabis method for the testing of the big four elements: Cadmium, Arsenic, Lead, and Mercury, and additional elements. Many of these elements are crucial to study because they play an important role in growth of the plant and plant byproducts. We looked at a variety of products, covering categories of Inhaled (Plant material, Vape Pen/cartridges, and Shatter), Oral (Pill, Tincture, and Edibles), Topical (Lotions, Oils, and Soaps), and Manufacturing (Biomass, Crude Extract, and Refined Extract) in the validation of this method. Presented by: Jenny Nelson(1), Craig Jones(1), Sam Heckle(2), and Leanne Anderson(2) (1) Agilent Technologies, Inc., 5301 Stevens Creek Blvd, Santa Clara CA 95051, U.S.; (2) CEM, Inc., 3100 Smith Farm Rd, Matthews, NC, 28104, U.S.

A Look at ISO/IEC 17025:2017 - Section 7.1 “Review of Requests, Tenders, and Contracts”

Presented by Perry Johnson Laboratory Accreditation

Common Findings in PJLA Assessments to the ISO/IEC 17025:2017 Standard in 2021

Presented by PJLA 

A Look at ISO/IEC 17025:2017 - Section 5.0 “Structural Requirements”

This section specifies broad encompassing requirements concerning documentation of laboratory activities, laboratory organization, structure, and responsibilities. This webinar will look each clause within Section 5 and highlight the flexibility given to laboratories in meeting these requirements. Presenter: Michael Kramer, PJLA Calibration Program Manager and Lead Assessor

Testing for Gluten and Allergens: Why We Do It and How To Do It Well

Presented by Perry Johnson Laboratory Accreditation