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.
Based on ISO 9001 but with nearly 100 additional requirements specific to the aerospace MRO industry, AS9110 provides suppliers with a comprehensive quality system focused on areas directly impacting product safety and reliability.
Audience: |
Beginner to Advanced |
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Schedule: |
Days 1-4: 7:30 AM – 6:30 PM MSTDay 5: 7:30 AM – 11:00 AM MST |
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| This course is certified by Probitas Authentication. Successful completion of this course satisfies the AS9110 Lead Auditor training requirement for Aerospace Auditor authentication.
Even though AS9110 is used as the model for teaching systems and audit, this course enables students to develop and apply auditing skills using any applicable management system standard. In addition to this course, aerospace auditors must also complete the IAQG sanctioned Aerospace Auditor Transition Training course to fulfill the training requirements for aerospace auditor authentication and recognition in OASIS. |
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OverviewOrganizations in the aerospace maintenance, repair, and overhaul (MRO) industry face unique quality requirements, and effective auditing is essential for maintaining compliance, managing risk, and ensuring safety. AS9110 builds on ISO 9001 by adding MRO-specific requirements that must be clearly understood and properly assessed during audits. This interactive, live-online AS9110 Lead Auditor Training equips you with the knowledge and practical skills to conduct, manage, and lead audits to both AS9110C and ISO 9001:2015 standards. Certified by Probitas, this course fulfills the formal training requirement for AS9110 Lead Auditors. Led by experienced instructors, you will explore every phase of the audit process, including:
This course emphasizes hands-on learning through interactive activities, group discussions, case studies, real-world scenarios, and role-playing exercises. Whether you are auditing internal processes, suppliers, or regulatory compliance, you will gain the confidence, knowledge, and tools needed to perform high-quality audits in MRO and aerospace service environments. You will also leave with a practical, structured, and repeatable approach to auditing that supports long-term success. |
Pre-RequisitesStudents will need to complete assignments before the start of class, including reading the standard. This AS9110 Lead Auditor training course is beneficial for both quality novices and lifetime professionals. Our goal is to meet everyone at their current level of competence and improve it. All students are required to bring their own copy of the AS9110 RevC standard. This will not be provided by Axeon, but most students will be able to obtain a copy from their company. |
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Who Should Attend
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| AS9100 Rev D Lead Auditor Training | AATT AS9100 IAQG Sanctioned Aerospace Auditor Transition Training | AS9102 First Article Inspection Training | AS9145 APQP & PPAP Training |
Audience: |
Beginner to Advanced |
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Schedule: |
Days 1-4: 7:30 AM – 6:30 PM Local TimeDay 5: 7:30 AM – 11:00 AM Local Time |
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| This course is certified by Probitas Authentication. Successful completion of this course satisfies the AS9110 Lead Auditor training requirement for Aerospace Auditor authentication.
Even though AS9110 is used as the model for teaching systems and audit, this course enables students to develop and apply auditing skills using any applicable management system standard. In addition to this course, aerospace auditors must also complete the IAQG sanctioned Aerospace Auditor Transition Training course to fulfill the training requirements for aerospace auditor authentication and recognition in OASIS. |
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OverviewIn the aerospace maintenance, repair, and overhaul (MRO) industry, compliance with AS9110C and ISO 9001:2015 is critical to ensuring quality, safety, and customer satisfaction. Auditors must be well-prepared to assess both general and MRO-specific requirements with precision and confidence. This in-person AS9110C Lead Auditor Training delivers a rich, immersive learning experience that goes beyond the screen. Certified by Probitas, this five-day course fulfills the formal training requirement for AS9110 Lead Auditors and equips you with the practical skills needed to conduct, manage, and lead internal, supplier, and regulatory audits. Held in a traditional classroom setting, this training allows for deeper engagement, real-time feedback, and dynamic peer interaction. You’ll benefit from direct access to instructors, group exercises, and collaborative discussions that mirror the challenges auditors face in the field. In this class, you will explore every phase of the audit process, including:
This course is highly interactive, using case studies, role-playing scenarios, and real-time coaching to build your competence and confidence. The in-person format enhances retention, fosters professional connections, and provides a hands-on environment ideal for building strong audit leadership skills. Whether you are advancing your career or supporting your organization’s certification goals, this training offers the structure, support, and in-depth instruction you need to succeed. |
Pre-RequisitesStudents will need to complete assignments before the start of class, including reading the standard. This AS9110C Lead Auditor training course is beneficial for both quality novices and lifetime professionals. Our goal is to meet everyone at their current level of competence and improve it. All students are required to bring their own copy of the AS9110C standard. This will not be provided by Axeon, but most students will be able to obtain a copy from their company. |
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Who Should Attend
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| AS9100 Rev D Lead Auditor Training | AATT AS9100 IAQG Sanctioned Aerospace Auditor Transition Training | AS9102 First Article Inspection Training | AS9145 APQP & PPAP Training |
Note:

OverviewWhen a single failure can ground a fleet or compromise safety, aerospace manufacturers must get risk management right the first time. AS13004 offers a proven, structured approach to identifying and controlling process risks before they result in costly nonconformities, escapes, or customer dissatisfaction. This focused, two-day AS13004 PFMEA Risk Management Training equips aerospace professionals with the tools and methods needed to identify, assess, and mitigate risk throughout the production process. This course directly supports compliance with AS9100, AS9120, and AS13004 by focusing on the practical application of PFMEA and Control Plan development as key elements of a proactive risk management strategy. Led by instructors with deep industry experience, this course covers:
Through case studies, interactive exercises, and detailed walkthroughs, participants will gain hands-on experience developing PFMEAs and Control Plans that reduce variability, improve product safety, and strengthen compliance across the aerospace supply chain. |
What You Will Learn
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Who Should Attend
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Days: 2
Time: 7:30 a.m.- 4:30 p.m. MST
As Root Cause CAPA for Aerospace, an AS13000 training is a must-have. If you are a Boeing, Airbus, or other top OEM supplier, you need this class! All suppliers for the top OEM’s are required to have an 8D Practitioner. This course fulfills the training and testing requirements to become an 8D Practitioner.
AS13000 defines the Problem-Solving standard for suppliers within the aero-engine sector, with the Eight Disciplines (8D) problem-solving method being the basis for this standard.
| This 2-day course provides students with a comprehensive and standardized set of tools to become an 8D practitioner and meets all the requirements of “training syllabus” (see AS1300 APPENDIX C). Successful application of 8D achieves robust corrective and preventive actions to reduce the risk of repeat occurrences and minimize the cost of poor quality. This is essential to enable long-term customer-supplier relationships and positively contributes towards zero defects and customer satisfaction.
This course includes the practical application of each of the 8D disciplines. |
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Learning Objectives:
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An AS13000 training is a requirement for Aerospace Suppliers of any top OEM. Any employees that will conduct a corrective action or participate as a team member, as well as any individual who would like to gain an in depth understanding of the 8-D process.
OverviewDeveloping a new product is a complex process that requires proactive planning, strong collaboration, and reliable controls to ensure quality from concept through delivery. Without the right structure in place, organizations face costly delays, supplier quality issues, and risks that can impact performance and customer satisfaction. Axeon’s AS9145 Advanced Product Quality Planning & Production Part Approval Process Training provides the framework needed to deliver aerospace products that meet requirements the first time. This course aligns with the AS9145 standard, which spans early concept development, design and process development, validation activities (PPAP), and post-delivery oversight. Participants will learn how these activities integrate with established aerospace quality standards, including AS9100, AS9102, AS9103, and AS9110. Through expert guidance and practical exercises, this two-day course helps teams enhance planning discipline, strengthen supplier management, and ensure product and process readiness before full-scale production. Attendees will gain a solid understanding of project phases, documentation requirements, approval expectations, and how to apply a risk-based approach throughout the product lifecycle. Delivered live in a virtual classroom environment, this instructor-led course includes hands-on workshops using industry tools such as SCMH checklists, real-world implementation examples, and a comprehensive case study. Whether you are overseeing production development, evaluating supplier readiness, or improving internal processes, this training equips you to reduce uncertainty, improve quality outcomes, and maintain compliance in today’s demanding aerospace environment. |
AS9145 APQP & PPAP Training Key Topics
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Who Should Attend
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OverviewEnsuring the quality and reliability of aerospace products starts with a thorough verification process. The AS9102 First Article Inspection (FAI) standard provides a consistent framework for documenting and verifying that products meet design specifications before full-scale production. Using this process can improve quality, reduce costs, and streamline schedules by eliminating unique organizational requirements and promoting best practices across the supply chain. Axeon’s AS9102 FAI training provides a practical, one-day online course designed for participants at all experience levels, from beginners to seasoned professionals. Attendees will learn when and how to apply the standard, complete the required forms, and interpret documentation requirements relative to their own procedures. The course emphasizes hands-on exercises, including evaluating drawings, reviewing completed FAIRs, and completing forms from source documents to ensure a deep understanding of both process and reporting requirements. Through guided instruction, interactive exercises, and real-world case studies, this online training equips participants with the skills needed to effectively implement FAI processes within their organization, improve product verification practices, and maintain compliance with aerospace quality standards. |
Pre-RequisitesThere are no required prerequisites for this training. This training course is beneficial for both quality novices and lifetime professionals. All students are required to bring their own printed or virtual copy of the AS9102 Rev C standard. This will not be provided by Axeon, but most students will be able to obtain a copy from their company. |
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Who Should Attend
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Days: 1 • CEU Hrs: 4.8
Time: 7:30 a.m.- 4:30 p.m. MST
Audience: Beginner to Advanced
Days: 1
Time: 7:30a.m.-4:30p.m. MST
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. An export license is a general term for both ITAR and EAR-controlled items in which the US Government has granted permission to transport or sell potentially dangerous items to foreign countries or parties.
To be ITAR or EAR compliant, a manufacturer or exporter whose articles or services appear on the USML or CCL lists must register with the U.S. State Department’s Directorate of Defense Trade Controls (DDTC). ITAR and EAR compliance can be problematic for a global corporation because the data related to a specific type of technology may need to be transferred over the Internet or stored locally outside the United States to make business processes flow smoothly. It is the responsibility of the manufacturer or exporter to take the necessary steps to certify that they are in compliance with the regulations.
Export control laws provide for substantial penalties, both civil and criminal. Failure to comply with ITAR can result in civil fines as high as $500,000 per violation, while criminal penalties include fines of up to $1,000,000 and 10 years imprisonment per violation. Under EAR, maximum civil fines can reach $250,000 per violation. Criminal penalties can be as high as $1,000,000 and 20 years imprisonment per violation.
The Department of State is responsible for the export and temporary import of defense articles and services governed by 22 U.S.C. 2778 of the Arms Export Control Act and Executive Order 13637. The International Traffic in Arms Regulations (“ITAR,” 22 CFR 120-130) implements the AECA.
The more stringent of the two sets of regulations was written for articles with direct defense-related applications. Articles specifically designed or otherwise intended for military end-use are enumerated on the United States Munitions List (USML) or the Missile Technology Control Regime (MTCR) Annex and therefore controlled by International Traffic in Arms Regulations (ITAR) which is administered by the Directorate of Defense Trade Controls (DDTC) at the State Department. Items, services, and information are all covered by the ITAR regulations. The most controlled items are Significant Military Equipment (SME) which have “capacity for substantial military utility or capability” such as tanks, high explosives, naval vessels, attack helicopters, etc which are noted on the USML with an asterisk. Some examples include; an export license (DSP-5), exchanging technical emails or teaching how to repair an ITAR-covered item which requires a Technical Assistance Agreement (TAA), and allowing a foreign company to manufacture an item requires a Manufacturing License Agreement (MLA).
Most other items not specifically listed in the USML, but with the capability to be used for either civilian or military purposes are considered “dual-use” and controlled under the Export Administration Regulations (EAR) which is administered by the Bureau of Industry and Security (BIS) at the Department of Commerce (DoC). The Commerce Control List (CCL) is the equivalent list at the DoC to the State Department’s USML. The CCL specifically controls for Chemical & Biological Weapons, Nuclear Nonproliferation, National Security, Missile Technology, Regional Stability, Firearm Convention, Crime Control, and Anti-Terrorism. The level of control depends on the country being exported to, destination party, end-use, and Export Control Classification Number (ECCN). Specifically, there are “600 Series” and “500 Series” items that are more strictly controlled than the rest of the CCL, but less strictly controlled than the articles on the USML.
This introductory course is for business executives, international contracting specialists, contract managers and administrators, program and project managers, marketing professionals, engineers, and other technical personnel, newly appointed export compliance officers, logistics personnel, and legal and financial advisors.
Days: 2
Time: 7:30 AM- 4:30 PM MST
Axeon’s training courses begin with your objectives in mind. Before any training begins the instructor must have an objective to deliver your desired outcome. If the course does not have a specific objective, students can go through the motions with little added value. Axeon’s Statistical Process Control training begins with a candid discussion of your needs and expectations with the course instructor to develop specific areas of focus for the class. Below is a general outline for the course and topics that will be covered.
Statistical process control (SPC) procedures help you monitor process behavior. One of the staple SPC tools used by quality process analysts, improvement associates, inspectors and more is the control chart. Axeon’s statistical process control training will walk you through the details of control charting and other SPC procedures and how to apply them within your organization.
| · Quality & Process Engineers | · Process Development & Validation Personnel |
| · Quality Technicians | · Manufacturing/Operations Personnel |
| · Production Supervisors | · Process Improvement Personnel |
| · SPC Supervisors | · Supplier Quality Personnel |
| · Laboratory Personnel | · Six Sigma Professionals |
Days: 2
Time: 7:30 AM- 4:30 PM MST
Audience: Beginner to Advanced
Human Factors is a term that appears in the latest versions of several ISO standards, including:
This Human Factors online training helps you to understand human factors in the context of each standard. You will learn how to apply the concept of human factors to your management system and address the standard requirements. You will also receive practical tools, proven methodologies, and helpful tips to make the job easier for you.
As with all of Axeon’s courses, this is a practical, how-to that is not bogged down in academic discussions. We use case studies, practice exercises, and learning activities to keep the training activities and build competence.
| · Quality managers | Also: |
| · Management representatives | · Quality consultants |
| · Quality engineers | · Those involved in performing corrective actions |
| · Safety managers | · Those involved in medical device risk management |
| · Top management | · Preparation Of Checklists From Process Analysis |
| · Regulatory affairs specialists | |
Prerequisites
None. Our students range from seasoned quality professionals to novices. Our goal is to meet everyone at their current level of competence and increase it.
Intro to Human Factors
Review ISO Standard Requirements: 9001, AS9100D, 14971, 45001
Definitions of Human Factors by Standard
Human Factors and Root Cause Analysis
Corrective Action and Human Factors
The 13 Most Common Human Factors
Activity: Applying Human Factors in Corrective Action
Human Factors and Poka-Yoke
Definition & History of Poka-Yoke
Methodology for Poka-Yoke
Activity: Applying Poka-Yoke to Human Factors
Human Factors and Health & Safety
Definition of Human Factors in Health & Safety
Human Factors and Ergonomics
How Human Factors influence Safety at Work
Activity: Applying Human Factors to Safety
Human Factors and Medical Devices
Methodology for Considering Human Factors in Risk Assessment
Device Design According to Human Factors Consideration
Human Factors in Post-Market Surveillance
Final Test
Days: 1
Time: 7:30 AM-4:30 PM MST
Audience: Top management
A QMS (Quality Management System) is NOT a cost of doing business. It’s an investment. And top management should expect to get a financial return on that investment. However, the Return On Investment (ROI) they receive will be greatly impacted by the level of leadership and commitment they provide concerning the management system.
The newest versions of most ISO management standards have amplified the requirements for top management, in accordance with ISO 9001:2015. In this highly interactive course, senior managers will learn how to fulfill their new responsibilities, take accountability, and maximize the ROI they get from their management systems.
This class will help to show the true value of your quality management system and how much it really adds to your bottom line. It will also help your company to increase the ROI of your QMS.
If you want to improve your company’s bottom line or show your boss how much your QMS is already contributing to profits then this class is for you.
Benefits of a Quality Management System
Overview of Quality Principles
How to Maximize the ROI from your QMS
The Five Biggest Mistakes Executives Make with Quality Management
Final Test
November 21, 2025 | 12:00 PM MT | 2:00 PM ET
Register Now