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The concept of a Quality System’s approach to business has been employed successfully and sometimes not so successfully for several decades. The International Organization for Standardization (ISO) has been supplying standards that list the key elements/clauses and requirements for building and implementing Quality Systems for over 30 years. These standards are based on the relatively simple concepts of Total Quality Management (TQM), essential principals of management, and a “Process” approach. These standards have been revised several times over the years to make them more realistic and user friendly.

Internal audits are a requirement of the AS9100, AS 13100 and RM 13005 and are intended to verify the compliance and effectiveness of an organization's quality management system. The methods and techniques for performing internal audits have significantly changed in the aviation, space and defense industries, and internal auditors must be knowledgeable of these requirements and the expectations as identified in the standard.

Crash reconstruction is a scientific process that utilizes principles of physics and empirical data to analyze the physical, electronic, video, audio, and testimonial evidence from a crash to determine how and why the crash occurred. This course will introduce this reconstruction process as it gets applied to various crash types - in-line and intersection collisions, pedestrian collisions, motorcycle crashes, rollover crashes, and heavy truck crashes. Methods of evidence documentation will be covered. Analysis methods will also be presented for electronic data from event data recorders and for video.

Individuals responsible for quality management system (QMS) implementation, preparation, realization, and auditing to the AS9100:2016 standard series for Aviation, Space, and Defense (ASD) require an understanding of International Aerospace Quality Group (IAQG) ASD standards requirements. When ASD standards are implemented and correctly maintained, utilizing the process approach, managing risks, and proactively identifying opportunities its use results in improved performance. An understanding of Certification Body requirements will have a direct impact on the outcome of the QMS audit as companies utilize AS9100 Rev. D.

Designed for individuals who are involved with quality management systems, implementation, and auditing to the AS9100D standard for Aviation, Space, and Defense, this course will provide an overview of the preparation for, and execution of the audit process as defined in this standard. This course provides training on the standard itself but also insights on how to lead or conduct internal audits and supplier audits. This course is authenticated by Probitas™ and qualifies for third-party auditor certification. It is taught by in-service, credentialed lead auditors. There is 40 hours of instructional time, followed by an exam.

Analysis of tolerance stacks varies widely. This web course introduces the basic tools to create a common methodology for tolerance stack-ups, and ensure seamless documentation. Participants will create 1-D tolerance stacks for parts and assemblies that use geometric dimensioning and tolerancing using a tolerance stack spreadsheet. This simple, manual spreadsheet method produces an easily interpreted and checked documentation trail, and is easily adaptable to common electronic spreadsheet programs. Multiple examples will be provided to assist engineers in applying tolerance stack-up fundamentals to Y14.5 issues.

IATF 16949:2016 is a technical specification for the automotive sector quality management systems, developed by the International Automotive Task Force (IATF), aimed at harmonizing the different supply chain assessment and certification systems worldwide. The IATF 16949:2016 standard incorporates applicable automotive customer-specific requirements and is a supplement to ISO 9000/9001:2015 requirements for automotive production and relevant service part organizations. 

ISO 13485:2016 is an international standard that establishes the requirements for a quality management system specific to the medical devices industry. It specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. ISO 13485 is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services.

ISO 13485:2016 is an international standard that establishes the requirements for a quality management system specific to the medical devices industry. It specifies requirements for a quality management system, and how to demonstrate compliance to meet customer and applicable regulatory requirements. ISO 13485 is designed to be used by organizations involved in the design, production, installation, and servicing of medical devices and related services. It can also be used by internal and external parties, such as certification bodies, to help them with their auditing processes.  Estimated to take up to 15-hours to complete.

Learn and understand the requirements of AS9100D, the process approach to managing an organization and the risk-management requirements. This course will cover the requirements of AS9100D and demonstrate how to interpret them within an organization. It is a first step in SAE’s AS9100D portfolio of courses and is appropriate for beginners and those with moderate knowledge of auditing management processes. Experienced auditors will also find value in the content provided. Estimated to take up to four hours to complete, this self-paced AS9100D Overview is geared toward the high-level requirements of this standard.

IATF 16949:2016 is a quality management standard, developed by the International Automotive Task Force (IATF), aimed at harmonizing the different supply chain assessment and certification systems worldwide. The IATF 16949:2016 standard is primarily applicable for the automotive industry, incorporates the new clause structure, and uses the content of ISO 9001:2015. The course includes ISO 9001:2015 quality management system requirements, ISO 19011:2018, the guideline to auditing quality systems, and points to the IATF 16949 requirements contained in the standard you will need to purchase from AIAG.

This self paced course reviews the important facets of ISO 9001:2015, the most widely accepted quality management standard.  The standard can be applied to any organization that, regardless of its type or size, needs to demonstrate its ability to consistently provide products and services that enhance customer satisfaction and provide assurance of conformity to customer and applicable statutory and regulatory requirements. Estimated to take up to 15 hours to complete,  this self paced course provides training on the standard, and how to lead or conduct internal audits and supplier audits using ISO 19011:2015.  

This course presents the requirements of AS9100D and demonstrates how to interpret them within an organization. Designed for individuals who are involved with quality management systems, implementation, and auditing to the AS9100:2016 series of standards for Aviation, Space, and Defense, this course will provide an overview of the preparation for and execution of the audit process as defined in these revised standards. Estimated to take up to 24 -hours to complete, this course provides training on the standard itself but also insights on how to lead or conduct internal audits and supplier audits using AS9100D.

ISO 14001:2015 is an environmental management standard (EMS) developed by the International Organization for Standardization (ISO). It’s a generic standard that can be used for any organization that provides physical products or services. ISO 14001 is the most widely used EMS because it’s both business and management oriented. However, the requirements must be carefully interpreted to make sense within a particular organization. For example, the environmental impact of developing automotive products is not the same as producing food products or offering consulting services, yet this standard can be applied to any of these activities.

Learn and understand the requirements of AS9100D, the process approach to managing an organization and the risk-management requirements. This course will cover the requirements of AS9100D and demonstrate how to interpret them within an organization. Designed for individuals who are involved with quality management systems, implementation, and auditing to the AS9100:2016 series of standards for Aviation, Space, and Defense, this course will provide the participant with an understanding of AS9100D, and knowledge related to the requirements for the preparation and execution of the audit process as defined in these revised standards.

This self paced course reviews the important facets of ISO 9001:2015, the most widely accepted quality management standard.  The standard can be applied to any organization that, regardless of its type or size, needs to demonstrate its ability to consistently provide products and services that enhance customer satisfaction and provide assurance of conformity to customer and applicable statutory and regulatory requirements. 

Learn and understand the requirements of AS9100D, the process approach to managing an organization and the risk-management requirements. This course will cover the requirements of AS9100D and demonstrate how to interpret them within an organization. Designed for individuals who are involved with quality management systems, implementation, and auditing to the AS9100:2016 series of standards for Aviation, Space, and Defense, this course will provide provides the participant with an understanding of the AS9100D standard, and knowledge related to the requirements for the preparation and execution of the audit process.

ISO 13485:2016 is an international standard that establishes the requirements for a quality management system specific to the medical devices industry. It specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. ISO 13485 is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services.