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Perry Johnson Laboratory Accreditation, Inc.

Laboratory Accreditation and Training Specialists

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Past Webinar Slides

Please fill out the form below to receives a copy of the slides from our past webinars:

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Select Past Webinar(s):
- I Submitted A Complaint: Why is this Organization Still Accredited?
- Use of Accreditation Symbols and References to Accreditation
- A Review of ISO/IEC 17025:2017 Requirements in Section 7.2 “Selection, Verification and Validation of Methods”
- A Look at ISO/IEC 17025:2017 – Review of Section 8.5 “Actions to Address Risks and Opportunities”
- A Look at ISO/IEC 17025: 2017 - Section 7.6 “Evaluation of Measurement Uncertainty” for Testing Laboratories
- Common Findings in Assessments to the ISO/IEC 17025:2017 Standard in 2022
- Best Lessons Learned from FDA Warning Letters
- Requirements for Personnel in ISO/IEC 17025:2017 Section 6.2
- Streamlining Laboratory Efficiency
- Section 8.8 Internal Audit Requirements
- Section 8.9 Management Review Requirements and Utilization
- A Look at ISO/IEC 17025 – Section 6.3 on Facilities and Environmental Conditions & Section 6.4 on Equipment
- Option A and B as Presented in ISO/IEC 17025:2017 Along with the Management System Documentation (8.2)
- A Look at ISO/IEC 17025:2017 – Section 7.9 “Complaints”
- A Look at ISO/IEC 17025:2017 – Section 6.5 Evaluation of Measurement Uncertainty “Requirements and Fundamentals”
- Common Findings Detected on Environmental Lab Assessments
- A Look at ISO/IEC 17025:2017 – Section 7.7 & Associated Requirements Within PL-1
- A look at the ISO/IEC 17025:2017 Requirements Concerning Document Control and Control of Records
- Improve your Force Measurements
- Section 7.8 of ISO/IEC 17025:2017 “Reporting of Results”
- The Metals in Cannabis Method with first action status by AOAC, the road to get there…
- ISO/IEC 17025:2017: Section 7.1 “Review of Requests, Tenders, and Contracts”
- Common Findings in Assessments to the ISO/IEC 17025:2017 Standard in 2021
- ISO/IEC 17025:2017: Section 5 “Structural Requirements”
- Testing for Gluten and Allergens: Why We Do It and How To Do It Well
- A Look at ISO/IEC 17025:2017: Section 7.10 “Nonconforming Work” & Section 8.6 “Improvement”
- ISO 17034:2016 General Requirements for the Competence of Reference Material Producers
- Overview of Key Requirements of ISO/IEC 17020:2012 “Inspection”
- ASCA Biocompatibility & Basic Safety & Essential Performance FDA Pilot Program
- ISO/IEC 17025:2017 Section 6.6 Externally Provided Products and Services
- 5 Steps to the Accreditation Process
- ISO/IEC 17025:2017 “Corrective Action 8.7”
- PJLA Policy on Measurement Uncertainty “PL-3”
- A Look at the Requirements Specified in PJLA Policy on Measurement Traceability “PL-2”
- Navigating Challenges Associated with PCR Technology in a Cannabis Laboratory
- A Look at the Requirements Specified in PJLA Policy on Proficiency Testing Requirements “PL-1”
- An Update to AOAC International Methods in the Cannabis Industry
- Other