Past Webinar Slides Please fill out the form below to receives a copy of the slides from our past webinars: Name:* First Last Company:* Phone:*Email:* 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