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9/12/2024	Uncertainty Propagation for Force with Henry Zumbrun
8/14/2024	ISO/IEC 17025:2017 Section 7.4 “Handling of Test or Calibration Items” & 7.11 “Control of Data and Information Management”
7/24/2024	A Summary of Changes of the DoD/DOE ELAP QSM Version 6.0 and PJLA Transition Requirements
5/30/2024	AOAC Hemp & Cannabis Proficiency Testing – A Solution to a Critical Need
4/30/2024	FDA Laboratory Accreditation for Analyses of Food (LAAF) Program: Lessons Learned
4/18/2024	A Look at ISO/IEC 17025:2017: Requirements Concerning Impartiality and Confidentiality
3/25/2024	A look at the ISO/IEC 17025:2017 Requirements Concerning Document Control and Control of Records
2/20/2024	Measurement Uncertainty & Decision Rules
1/19/2024	Common Findings in Assessments to the ISO/IEC 17025:2017 Standard in 2023
12/20/2023	Adding DOECAP-AP Accreditation to a DoD-ELAP Accredited Laboratory
11/30/2023	A Look at ISO/IEC 17025:2017 – Section 6.6 – Externally Provided Products and Services
10/31/2023	Understanding the PJLA Flexible Scope Policy for Testing Labs, RMPs, and PTPs
10/26/2023	A Look at ISO/IEC 17025:2017 – Overview of the Requirements Specified for Equipment in Section 6.4
9/28/2023	Measurement Risk: Measurements Gone Wrong
8/10/2023	A Look at ISO/IEC 17025:2017 – Requirements for Corrective Action
6/27/2023	A Review of the Revised PJLA Policy PL-4 “Scopes of Accreditation”
6/13/2023	Understanding the Types of Reference Materials, Their Differences, and Their Uses
5/31/2023	I Submitted A Complaint: Why is this Organization Still Accredited?
5/18/2023	Use of Accreditation Symbols and References to Accreditation
4/27/2023	A Review of ISO/IEC 17025:2017 Requirements in Section 7.2 “Selection, Verification and Validation of Methods”
3/29/2023	A Look at ISO/IEC 17025:2017 – Review of Section 8.5 “Actions to Address Risks and Opportunities”
2/21/2023	A Look at ISO/IEC 17025: 2017 – Section 7.6 “Evaluation of Measurement Uncertainty” for Testing Laboratories
1/27/2023	Common Findings in Assessments to the ISO/IEC 17025:2017 Standard in 2022
1/17/2023	Best Lessons Learned from FDA Warning Letters
12/22/2022	Requirements for Personnel in ISO/IEC 17025:2017 Section 6.2
12/6/2022	Streamlining Laboratory Efficiency
11/28/2022	Section 8.8 Internal Audit Requirements
10/28/2022	Section 8.9 Management Review Requirements and Utilization
9/26/2022	A Look at ISO/IEC 17025 – Section 6.3 on Facilities and Environmental Conditions & Section 6.4 on Equipment
8/29/2022	Option A and B as Presented in ISO/IEC 17025:2017 Along with the Management System Documentation (8.2)
7/25/2022	A Look at ISO/IEC 17025:2017 – Section 7.9 “Complaints”
6/30/2022	A Look at ISO/IEC 17025:2017 – Section 6.5 Evaluation of Measurement Uncertainty “Requirements and Fundamentals”
6/14/2022	Common Findings Detected on Environmental Lab Assessments
5/31/2022	A Look at ISO/IEC 17025:2017 – Section 7.7 & Associated Requirements Within PL-1
4/29/2022	A look at the ISO/IEC 17025:2017 Requirements Concerning Document Control and Control of Records
4/19/2022	Improve your Force Measurements
3/31/2022	Section 7.8 of ISO/IEC 17025:2017 “Reporting of Results”
3/24/2022	The Metals in Cannabis Method with first action status by AOAC, the road to get there…
2/22/2022	ISO/IEC 17025:2017: Section 7.1 “Review of Requests, Tenders, and Contracts”
1/24/2022	Common Findings in Assessments to the ISO/IEC 17025:2017 Standard in 2021
12/30/2021	ISO/IEC 17025:2017: Section 5 “Structural Requirements”
12/14/2021	Testing for Gluten and Allergens: Why We Do It and How To Do It Well
11/22/2021	A Look at ISO/IEC 17025:2017: Section 7.10 “Nonconforming Work” & Section 8.6 “Improvement”
10/27/2021	ISO 17034:2016 General Requirements for the Competence of Reference Material Producers
10/20/2021	Overview of Key Requirements of ISO/IEC 17020:2012 “Inspection”
10/18/2021	ASCA Biocompatibility & Basic Safety & Essential Performance FDA Pilot Program
9/29/2021	ISO/IEC 17025:2017 Section 6.6 Externally Provided Products and Services
9/23/2021	5 Steps to the Accreditation Process
8/30/2021	ISO/IEC 17025:2017 “Corrective Action 8.7”
7/23/2021	PJLA Policy on Measurement Uncertainty “PL-3”
6/28/2021	A Look at the Requirements Specified in PJLA Policy on Measurement Traceability “PL-2”
6/10/2021	Navigating Challenges Associated with PCR Technology in a Cannabis Laboratory
5/27/2021	A Look at the Requirements Specified in PJLA Policy on Proficiency Testing Requirements “PL-1”
5/13/2021	An Update to AOAC International Methods in the Cannabis Industry
5/7/2021	An Overview of the CA ELAP Regulations Versus the TNI EL 2016 Standard
4/26/2021	ISO/IEC 17025;2017, Section 4.1 Impartiality and 4.2 Confidentiality
3/25/2021	Use of Accreditation Symbols and References to Accreditation
2/23/2021	ISO/IEC 17025:2017 Section 7.4 “Handling of Test or Calibration Items” & Section 7.11 “Control of Data and Information Management”
1/25/2021	ISO/IEC 17025:2017 “Personnel”
12/30/2020	ISO/IEC 17025:2017 7.6 & 7.7 – Evaluation of Measurement Uncertainty & Validity of Results
12/8/2020	Preparing for an ISO/IEC 17025:2017 Accreditation Assessment
11/23/2020	ISO/IEC 17025:2017 and Section 8.8 on Internal Audits
10/29/2020	ISO/IEC 17025:2017 Section 8.9 Management Review Requirements and Utilization
9/29/2020	Common Findings in Assessments to the ISO/IEC 17025:2017 Standard
8/26/2020	Section 8.7 on Corrective Action
7/24/2020	Section 6.3 on Facilities and Environmental Conditions Along With Section 6.4 on Equipment
6/25/2020	Option A and B as presented in ISO/IEC 17025:2017
5/12/2020	Actions to Address Risk Opportunity
5/7/2020	Cannabis Potency II: An Second Example of Applying ISO 17025 Principles to a Test Method
4/20/2020	Cannabis and Hemp Industry Expert Webcast
4/20/2020	ISO/IEC 17025:2017 Requirements Concerning Document Control and Control of Records
4/15/2020	Fundamental Concepts For Developing Measurement Uncertainty Estimates – Short Course
4/13/2020	Cannabis Potency: An Example of Applying ISO 17025 Principles to a Test Method
3/31/2020	PJLA Overview – Virtual Remote Assessments
3/19/2020	ISO/IEC 17025:2017 Section 7.9 Complaints
2/28/2020	Section 7.8 of ISO/IEC 17025:2017 Reporting of Results
1/24/2020	ISO/IEC 17025:2017 “Ensuring the Validity of Results”
12/20/19	Overview of Differences Between ISO/IEC 17025:2005 & ISO/IEC 17025:2017
10/25/19	ISO/IEC 17025:2017, Section 4.1 Impartiality and 4.2 Confidentiality
9/20/19	Decision Rules and their application to meeting the requirements of ISO/IEC 17025:2017
8/29/19	Common Findings ISO/IEC 17025:2017
7/25/19	Section 5.0 “Structural Requirements” of ISO/IEC 17025:2017
6/27/19	ISO/IEC 17025:2017 Section 7.10” Nonconforming Work” & Section 8.6 “Improvement”
5/28/19	Section 7.4 “Handling of Test or Calibration Items” & Section 7.11 “Control of Data and Information Management”
4/25/19	ISO/IEC 17025:2017 “Personnel”
3/28/19	Traceability Requirements of ISO/IEC 17025:2017 and PJLA Policy on Measurement Traceability PL-2
2/21/19	ISO/IEC 17025:2017 Section 8.7 “Corrective Action”
1/24/19	ISO/IEC 17025:2017 Section 6.6 Externally Provided Products and Services
6/28/18	Actions to Address Risk and Opportunities “A look at Section 8.5 of ISO/IEC 17025:2017”
5/22/18	Statements of Conformity “ISO/IEC 17025: 2017 – 7.8.6 – Reporting Statements of Conformity to Include the Decision Rule”
3/29/18	ISO/IEC 17025 “A Glimpse at the Differences between ISO/IEC 17025:2017 & ISO/IEC 17025:2005”