Did you know that almost one-half of the DOE Consolidated Audit Program - Accreditation Program (DOECAP-AP) laboratories perform routine and project specific non-radiological analysis? There are opportunities for non-radiochemistry laboratories to support projects involving routine compliance monitoring, site characterization, process control testing, and remediation for various environmental matrices for the DOE. It is also anticipated PFAS analysis will exceed current non-radiological laboratory capacity in the near future. This webinar will review the anticipated differences between DOECAP-AP and DoD ELAP to the combined DoD/DOE Quality Systems Manual (QSM 6.0). The transition is not as difficult as it seems! We will identify less than twenty clauses of the QSM requiring laboratory consider or update. Our review will give laboratories the necessary Information to evaluate the opportunities to seek accreditation for DOECAP-AP for either the entire, or partial scope of DoD-ELAP accreditation in order to provide non-radiological analysis to the DOE. Presented by Matthew Sica, PJLA Technical Program Manager
A Look at ISO/IEC 17025:2017 - Section 8.9 Management Review Requirements and Utilization
A Look at ISO/IEC 17025 - Section(s) 6.3 & 6.4
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”
ISO/IEC 17025 Section 7.6 - Evaluation of Measurement Uncertainty
Common Findings Detected on Environmental Lab Assessments
A Look at ISO/IEC 17025:2017 - Section 7.7 & Associated Requirements Within PL-1
Improve Your Force Measurements: Tips to Improve Your Force Measurements
A Look at ISO/IEC 17025:2017 - Section 7.8 “Reporting of Results”
The Metals in Cannabis Method with first action status by AOAC & The Road to Get There…
A Look at ISO/IEC 17025:2017 - Section 7.1 “Review of Requests, Tenders, and Contracts”
Common Findings in PJLA Assessments to the ISO/IEC 17025:2017 Standard in 2021
A Look at ISO/IEC 17025:2017 - Section 5.0 “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 6.6: Externally Provided Products and Services
ASCA Biocompatibility and Basic Safety and Essential Performance FDA Pilot Program with PJLA
ISO 17034:2016 General Requirements for the Competence of Reference Material Producers
A Look at ISO/IEC 17025 2017 - Section 7.10 - Nonconforming Work Section 8.6 - Improvement
5 Steps to the Accreditation Process with Tracy Szerszen
A Look at the Requirements Specified in PJLA Policy on Measurement Uncertainty PL 3
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