STAT-A-MATRIX
Dallas, Las Vegas, United States
http://www.statamatrix.com

Internal Auditor Training for AS9100

We will teach you the steps to develop, implement, and audit an internal quality system that meets the requirements of ISO 9001:2000, AS 9100, and the needs of your organization in the most effective, efficient way. Make sure your training comes from the industry leaders¡ªSTAT-A-MATRIX has been training auditors longer than any other training organization in the world. This version of our RABQSA......
 

Learn how to assess compliance with ISO 9001:2000 and AS 9100 from the industry experts. Based on our ISO 9001:2000 RABQSA-certified IATCA QMS lead auditor training course, this interactive version covers the ISO 9001:2000 and AS 9100 requirements for quality management systems. Take your lead auditor training from the industry experts¡ªSTAT-A-MATRIX has been training lead auditors longer th......
 

This interactive two-day program provides you with an understanding of TL 9000 measurements and the means necessary to collect, prepare, analyze, and report the data. TL 9000 registration requires conformity to the TL 9000 Quality Management System Requirements, which includes reporting the TL 9000 quality system measurements data to the QuEST Forum Measurements Administrator. This course i......
 

Learn the steps necessary for successful implementation of TL 9000 quality management system requirements and measurements in this interactive program. Whether you have a mature quality system in place, or one under development, we will provide you with a roadmap for successful TL 9000 implementation and compliance. If you are currently a telecommunications industry supplier or planning to ......
 

Learn how to ¡°bridge the gap¡± between ISO 9001 and the additional requirements of TL 9000 from the perspective of an auditor. Step-by-step, auditors of the TL 9000 requirements learn how to interpret and understand the specific requirements of TL 9000, and how to effectively audit to verify compliance. Discussions cover TL 9000 measurements and the means necessary to measure ongoing performance......
 

This comprehensive overview of the ISO 14001:2004 Environmental Management System (EMS) Standard examines the language and intent of the stated requirements. It provides a foundation upon which additional levels of activity, from initial system design, through implementation and maintenance, to review and continual improvement, can be built. Participants engage in a series of interactive, ha......
 

Learn what your company needs to develop and implement a process-based internal audit program in accordance with ISO 19011, and the requirements of ISO/TS 16949:2002. This version of our RABQSA-certified internal auditor course includes discussion of key automotive requirements (APQP, PPAP, SPC, MSA, and FMEA) and how to make sure you design the most effective and efficient internal audit progr......
 

Understand the requirements of ISO/TS 16949:2002 (the international automotive sector-specific adaptation of the ISO 9001:2000 Quality Management System Standard) and how they differ from the prior automotive sector-specific quality standards including QS-9000 and ISO/TS 16949:1999. Ensure that your organization develops, implements, and maintains an effective QMS that will realize the qual......
 

Get the information you need to understand the ISO 13485:2003 and ISO 9001:2000 standards and how they impact your organization. Dynamic group discussions focus on when compliance or registration is required or desirable, how to document and design an effective quality management system, what the revised requirements mean for the worldwide medical device industry, and what auditors are looking ......
 

Get the latest information on risk management concepts and practices for the medical device industry and learn how to plan your organization¡¯s risk management and analysis program. Understanding risk analysis is essential to anyone in the medical device industry¡ªthis is a focus of the design control requirements in FDA¡¯s Medical Device Quality System Regulation and ISO 14971: Application of Ris......
 

Using careful reviews of requirements from ISO 9001:2000, ISO 13485 and QSR along with case studies and in-class activities, learn the fundamentals and principles of process validation. Focus is on the planning, specifications, and requirements necessary to meet ISO and FDA requirements for process validation. FDA defines process validation as ¡°establishing documented evidence which provides a ......
 

Using case studies and in-class activities, learn the critical concepts and principles of process validation. Focus is on the basic concepts, techniques, and requirements necessary to meet current FDA expectations for process validation. FDA defines process validation as ¡°establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce......
 

Learn the steps to develop, implement, and audit an internal quality system that efficiently and effectively meets the requirements of ISO 13485:2003 and ISO 9001:2000. Get your training from the industry leaders¡ªSTAT-A-MATRIX has been training auditors longer than any other training organization in the world. This version of our RABQSA-certified internal auditor course includes workshops tailo......
 

FDA-regulated organizations must establish and maintain a quality system appropriate for the specific medical device being manufactured and meet the requirements of FDA¡¯s Medical Device Quality System Regulation. QSIT is intended to increase manufacturer compliance, inspectional consistency, product quality, and the efficiency of the enforcement action review process. Review guidelines for t......
 

Has your organization documented the flow of the design process so it is clear to an FDA inspector where your research ends and design development begins? FDA has identified design control as a key area in its QSIT top-down inspectional approach of compliance. According to the FDA, ¡°Manufacturers must incorporate a set of checks and balances in their design processes to assure a safe, effective......
 

Learn how to assess compliance with ISO 9001:2000 and ISO 13485:2003 from the industry experts. Based on our ISO 9001:2000 RABQSA-certified IATCA QMS lead auditor training course, this interactive course covers the ISO 13485:2003 and ISO 9001:2000 requirements for quality management systems. Get your lead auditor training from the seminar experts¡ªSTAT-A-MATRIX has been training lead auditor......
 

Learn how to assess compliance with ISO 9001:2000 from the industry experts. STAT-A-MATRIX has been training lead auditors longer than any other training organization in the world. Our ISO 9001:2000 RABQSA-certified IATCA auditor/lead auditor training course, presented largely through hands-on workshops, teaches you the skills you need to plan, conduct, and follow-up on ISO 9001 compliance audi......
 

We will teach you the steps to develop, implement, and audit an internal quality system that meets the requirements of ISO 9001:2000 and the needs of your organization. Get the training you need from the industry¡¯s leader¡ªSTAT-A-MATRIX has been training auditors longer than any other training organization in the world. Our RABQSA-certified internal auditor course includes interactive workshops ......
 

Corrective and preventive action (CAPA) requirements for ISO 9001:2000 registered/compliant companies must be understood and implemented effectively. CAPA systems should provide critical input to top management relative to the status of the continuing effectiveness of the Quality Management System (QMS) and the efficiency and profitability of the organization. Objectives Understand the IS......
 

Eliminate waste in your processes by implementing lean in your organization.This set of approaches, methods, and tools is based on the world¡¯s most efficient manufacturing technology¡ªthe Toyota Production System.It can help any kind of organization improve, including service, government, and nonprofit organizations. Based on standardized management deployment systems and starting with the lean ......
 

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