Use the best practices that AS9110 C provides to not only demonstrate commitment for providing continuously-improved aerospace parts and services, but globally apply your quality management…

Although the ISO 9001 requirements have been removed from IATF 16949:2016 and are published as a separate ISO standard, IATF 16949 is not a stand-alone standard and must be used in…

Although the ISO 9001 requirements have been removed from IATF 16949:2016 and are published as a separate ISO standard, IATF 16949 is not a stand-alone standard and must be used in…

AS9100 uses all the ISO 9001 standards as a foundation, building on additional regulatory requirements and notations pertaining specifically to aerospace quality needs. AS9100 is backed by…

AS9100 uses all the ISO 9001 standards as a foundation, building on additional regulatory requirements and notations pertaining specifically to aerospace quality needs. AS9100 is backed by…

Learn how to interpret the 13485 Standard and apply it to your own organization. This course prepares you to perform effective audits of Medical Device Quality Management Systems. Within…

This seminar fully covers the ISO 13485:2016 requirements. Auditing topics from ISO 19011 such as the auditing process and methodologies, e. g. planning and conducting an audit,…

This IRCA certified course (certificate 17082) fulfills training requirements for Lead QMS Auditors (or lower levels). It focuses on developing your auditing skills for laboratories…

This 5-day course was designed for you to Learn the requirements of ISO 14001:2015 and ISO 45001:2018 and how to relate the requirements to your integrated management system. ACCESS…

The ISO 9001: 2015 standards as a foundation, building on additional regulatory requirements and notations pertaining to general manufacturing needs. Even though ISO 9001:2015 is used as…

The ISO 9001: 2015 standards as a foundation, building on additional regulatory requirements and notations pertaining to general manufacturing needs. Even though ISO 9001:2015 is used as…

The new ISO 17025:2017 standard aligns with ISO 9001:2015, making laboratory management systems easier to implement and improving the recognition of test and calibration results across…

This course is designed for organizations that require a systematic approach to risk identification, assessment, and management. This includes companies subject to the stringent…

AS13100 standard creates a common set of supplemental requirements with common training and reference manuals to improve your quality management system through understanding, and…

AS9100 uses all the ISO 9001 standards as a foundation, building on additional regulatory requirements and notations pertaining specifically to aerospace quality needs. Instead of being…

AS9100 uses all the ISO 9001 standards as a foundation, building on additional regulatory requirements and notations pertaining specifically to aerospace quality needs. AS9100 is backed by…

AS9100 uses all the ISO 9001 standards as a foundation, building on additional regulatory requirements and notations pertaining specifically to aerospace quality needs. AS9100 is backed by…

Applicable to all tiers of the global supply chain, this standard establishes a unified approach to first article inspection (FAI) processes and documentation. This harmonization ensures…

This two-day course provides participants with awareness and understanding of the requirements of the Cyber Security Maturity Model Certification (CMMC) and NIST SP800-171. The intent of…

This seminar equips participants with the tools to understand mechanical drawings. While some may have a natural talent for visualizing 3D objects from 2D drawings, this skill is attainable…

To better define a product to a customer or supplier, Geometric Dimensioning and Tolerancing (GD&T) is often used as a symbolic way of showing specific tolerances on drawings. GD&T…

Geometric Dimensioning and Tolerancing (GD&T) is a valuable tool that effectively communicates the design intent to manufacturing and inspection. To better define a product to a…

International Traffic in Arms Regulation: Export Control Regulations run by different departments of US Government. This course will provide company employees with an introduction to the…

Medical device auditing requires technical knowledge as well as a deep understanding of international medical device regulations. Students participating in this course will gain knowledge…

Learn how to interpret the 13485 Standard and apply it to your own organization. This course prepares you to perform effective audits of Medical Device Quality Management Systems. Within…

This seminar fully covers the ISO 13485:2016 requirements. Auditing topics from ISO 19011 such as the auditing process and methodologies, e. g. planning and conducting an audit,…

Learn the application of the FMEA approach to ISO 14971:2019 Application of Risk Management to Medical Devices, and be able to define the use of DFMEAs as a process within your…

This seminar is designed for: employees in charge of developing a risk management program for their organization and Individuals responsible for identifying and managing risk and…

The ISO 9001 and IA9100 transition training for quality management is designed to provide participants with an understanding of the changes happening to AS9100 Rev D and the ISO 9001…

The ISO 9001: 2015 standards as a foundation, building on additional regulatory requirements and notations pertaining to general manufacturing needs. Even though ISO 9001:2015 is used as…

This course provides participants with awareness and understanding of the requirements of the TISAX information security assessment maturity model (ISA released by the VDA) and illustrates…

ISO 27001 adopts the High-Level Structure of IATF 16949 and ISO 14001 and can be integrated into the same management system. The differences are in the required risk analysis and…

This 4-day course has been developed to cover all requirements of the ISO/IEC 27001:2022 standard. The course includes definitions from ISO/IEC 27000:2018 (Information Security Management…

WHAT YOU'LL LEARN: Acquire the activities to support vehicle cybersecurity for management, development, operation and more Learn how to implement ISO/SAE 21434 Ensure correct…

WHAT YOU'LL LEARN: Understand Aerospace NADCAP AC7102 Heat Requirements Implement and audit the requirements Organize for 3rd party special audits ACCESS TRAINING BROCHURE FOR…

WHAT YOU'LL LEARN: Understand Aerospace NADCAP AC7108 Chemical Requirements Implement and audit the requirements Organize for 3rd party special audits ACCESS TRAINING BROCHURE…

WHAT YOU'LL LEARN: Understand Aerospace NADCAP AC7114 Non Destructive Testing Requirements Implement and audit the requirements Organize for 3rd party special audits ACCESS…

WHAT YOU'LL LEARN: Understand and Explain all the different entries on an 8D. Demonstrate the ability to complete 8D report. Practice those tools and techniques learned. Practice…

This training is designed to provide participants with an understanding of how the risk management elements of Aerospace Advanced Product Quality Planning (APQP) help ensure successful…

This three-day course was developed to cover all requirements of the ISO/IEC 27001:2022 standard. The course includes definitions from ISO/IEC 27000:2018 (Information Security Management…

Medical device auditing requires technical knowledge as well as a deep understanding of international medical device regulations. Students participating in this course will gain knowledge…

Considering the ISO 13485:2016 management system requirements and various regulatory authorities compliance requirements around the world and the global supply chains involved, a…

Understanding MDSAP training course will teach students to plan, develop and implement a QMS in accordance with MDSAP and ISO 13485:2016 requirements. Considering the ISO 13485:2016…

This two-day seminar upgrades you on the latest ISO standard for testing and calibration labs (ISO/IEC 17025:2017) and highlights how a management system aligned with ISO 9001:2015 improves…