The IAQG-sanctioned 9100:2016 AATT has been mandated by the IAQG to satisfy the Foundation Course training requirement for 9100:2016 AQMS auditor authentication. The 9100 Online Component includes the ISO 9001:2015 Pre-Assessment, Foundations: Understanding 9100 Online Training, 9100:2016 Forms and Audit Reporting Training, and Trial Assessment Scenario 1 and 2. The four-day instructor-led portion of the AATT training focuses on applying the 9100:2016 requirements in audit situations using 9101:2016 forms and in consideration of 9101:2016 requirements. The fourth day of the instructor-led course is reserved for the final examination. Refer to the “Program Overview” section below for more information.
AS9110 is a standard that defines the quality system requirements for organizations whose primary business is in the aircraft industry at all levels of the maintenance, repair & overhaul (MRO) process. It is focused on the control of repair schemes and maintenance plans, configuration management, and the skills and qualifications necessary to perform MRO tasks within the aerospace community.
ISO 9001 is the international standard that specifies requirements for a quality management system (QMS). Organizations use the standard to demonstrate the ability to consistently provide products and services that meet customer and regulatory requirements.
AS9100 Rev D Trainings
AS9100 is the quality management standard specifically written for the Aerospace and Defense industry. Among the most safety-conscious in the world, the aerospace industry has long recognized the crucial role quality plays in the performance of aviation, space and defense products. Consumer and customer confidence is directly linked to perceptions about the quality of equipment and services manufacturers in this industry offer.
ISO 13485:2016 sets out the requirements for a quality management system specific to the medical devices industry. Improvements in the latest version of the standard include broadening its applicability to include all organizations involved in the life cycle of the product, from concept to end of life, greater alignment with regulatory requirements, and a greater focus on post-market surveillance including complaint handling.
What is CAPA? Corrective action and preventive action are improvements to an organization’s processes taken to eliminate causes of non-conformities or other undesirable situations.
Why is Risk Management Important? Risks affecting organizations can have consequences in terms of economic performance and professional reputation, as well as environmental, safety and societal outcomes. Therefore, managing risk effectively helps organizations to perform well in an environment full of uncertainty.
If you’ve looked up the definition for human factors on the internet, you’re probably still confused. That’s because each standard uses this term in a different context and contains its own unique requirements. Human factors is actually a fascinating topic that can benefit your root cause analysis, safety, and risk management processes.
What are ITAR and EAR? ITAR (International Traffic in Arms Regulations) and the EAR (Export Administration Regulations) are export control regulations run by different departments of the US Government. Both of them are designed to help ensure that defense-related technology does not get into the wrong hands.
ISO 14001:2015 specifies requirements for an environmental management system to enable an organization to develop and implement a policy which objectives take into account legal requirements as well as other requirements for which the organization subscribes with information about significant environmental aspects.
ISO 45001 Occupational Health and Safety Lead and Internal Auditor Trainings
What is ISO 45001?ISO 45001 is an ISO standard for management systems of occupational safety and health (OHSMS), published in March 2018. The goal of ISO 45001 is the…
Nadcap is an industry-managed approach to conformity assessment that brings together technical experts from both Industry and Government to establish requirements for accreditation, accredit Suppliers and define operational program requirements. This standardized approach to quality assurance reduces redundant auditing…
Maximizing the ROI from your Quality Management System
Axeon knows how valuable your position is. Does your boss know how much you do to affect your company profits? Our guess is your boss doesn’t. After attending this class, they will…
CMMC is a unifying standard for the implementation of cybersecurity across the Defense Industrial Base (DIB). The CMMC framework includes a comprehensive and scalable certification element to verify the implementation of processes and practices associated with the achievement of a cybersecurity maturity level.
IATF 16949 Automotive Lead and Internal Auditor Trainings
How has IATF 16949:2009 changed? The new Automotive Quality Management System requirements have been rebranded as IATF 16949:2016 (formerly ISO/TS 16949:2009). Although the ISO 9001 requirements have been removed from IATF…
FSSC ISO 22000 Food Safety Lead and Internal Auditor Trainings
What is FSSC ISO 22000? FSSC 22000 contains a complete certification scheme for Food Safety Management Systems based on existing standards for certification including ISO 22000, ISO 22002 specifications food-sector PRP…
NQA-1 Nuclear Quality Assurance Lead Auditor Training
NQA-1 (Nuclear Quality Assurance-1) is a regulatory standard created and maintained by ASME (American Society of Mechanical Engineers). The current version was released in 2019 (NQA-1-2019.)
ISO 17025 Lead and Internal Auditor Trainings
What is ISO/IEC 17025:2005?
ISO/IEC 17025:2005 specifies the general requirements for the competence to carry out tests and/or calibrations, including sampling. It covers testing and calibration performed using standard methods, non-standard methods,…
May 2, 2025 | 12:00-1:00 PM MST | 2:00-3:00 EST
Register Now
Location
Register
Login