Most self-paced IAS Training Courses are now free – Take your pick from the growing list below!

The Laboratory QA/QC Standard (ISO/IEC 17025):

• Changes within the 2017 version of ISO/IEC 17025
• Decision Rule in ISO/IEC17025

Webinar 1 – Accreditation vs. Certification? Which one should I choose?

Webinar 2 – The Route to Accreditation

Webinar 3 – Implementing Efficient Management Systems

Webinar 4 – How to Conduct an Effective Internal Audit

   Webinar 5 – Management Reviews Simplified

Webinar 6 – Corrective Actions, Learning from our Mistakes

Webinar 7 – Understanding Measurement Uncertainty

  Webinar 8 – Risks and Opportunities – Risk-based Thinking in Management System

Webinar 9 – What is Decision Rule and why should Laboratories care?

                                                                              Webinar 10 – Easy ways to Establish Competence of Lab Personnel

                                                                              Webinar 11 – How to Identify Valid Certificates

Webinar 12 – The Wheel of Fortune of Non – Conformities

Module 1 – ISO 15189 – Resource and infrastructure requirement for competence in a medical / clinical laboratory

Module 2 – ISO 15189 – Method and Process requirements

Module 3 – ISO 15189 – Process Management – Outcomes – Technical Requirements

Module 4 – ISO 15189 – System Management Policies – What is required?

Module 5 – ISO 15189 – Requirements and Procedures for Records

Module 6 – ISO 15189 – QA and QC in the Clinical Lab

Module 7 – ISO 15189 – Auditing Clinical Lab Processes

Module 8 – ISO 15189 – Measurement Traceability of all Laboratory Measurements

IAS Assessor Training for US EPA Energy Star

Calibration Assessor Seminar

2022 World Accreditation Day – Sustainability in Economic Growth and the Environment

2021 World Accreditation Day – Sustainable Development Goals

2021 World Metrology Day – What is it and why is it important?

2020 World Accreditation Day – Food Safety

Webinar 1 – 2016 ELAP Standard for Testing

Webinar 2 – California ELAP Regulations

Webinar 3 – How to Prepare for an ELAP Assessment

Webinar 4 – The Importance of QC in the ELAP Lab

Webinar 5 – Technical Criteria for Chemistry Methods and Equipment

Webinar 6 – Technical Criteria for Microbiology Methods and Equipment

Webinar 7 – Guidelines for Method Selection and Validation

Webinar 8 – Metrological Traceability in an ELAP Lab

Webinar 9 – Training and Competence Laboratory Personnel in an ELAP Lab

Webinar 10 – Creating and Integrating the Laboratory Quality Manual

Webinar 11 – Effective Internal Audits and Management Reviews in an ELAP Lab

Webinar 12 – Corrective Actions in the ELAP Lab

Webinar 13 –  Implementing a Robust Data Integrity Program in an ELAP Lab

Webinar 14 – Confessions of an ELAP Laboratory Assessor

Webinar 15 – Quality Management System Implementation for Small Laboratories

Webinar 16 – Implementing Effective Document Control in the ELAP Lab

Webinar 17 – Ensuring Qualified Suppliers and Subcontractors in an ELAP Lab

Webinar 18 – Management Requirements for ELAP Laboratories

Webinar 19 – Equipment Requirements for ELAP Laboratories

Webinar 20 – Sample Integrity in an ELAP Lab

Webinar 21 – Writing Effective Responses to an ELAP Assessment Report

Webinar 22 – Customer Service Requirements in an ELAP Lab

Webinar 23 – Method Detection Limits in an ELAP Laboratory

Webinar 24 – Policies and Procedures Required in an ELAP Laboratory

Webinar 25 – TNI Standard Interpretations for a CA ELAP Lab

Need for Full Corrective Action or Preventive Action or Neither

AC473 Cold-Formed Steel Component Manufacturer Inspection Accreditation