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Improving Performance, Reducing Risk
Quality management systems
LRQA provides a number of training solutions tailored to meet your needs and to ensure that you get the most out of your Quality Management System.
Your will require this training course if you are an internal auditor working in the automotive industry, whose QMS conforms to, or is developing towards the latest version of IATF 16949:2016 standard.
Maximize your learning and your time when you take advantage of an additional day of insight through dynamic Audit and Business Improvement training. Save $595 by selecting this combined course.
This one (1) day course is ideal for those who want a thorough understanding of ISO 9001:2015. Course content includes the eight principles of quality management, model for a process based management systems, requirements of ISO 9001:2015, and managing processes with the goal of improving business performance.
An Appreciation courses provides you with the foundational information to understand quality management systems and how process effectiveness directly links with business performance and in an Internal Audit course, you’ll learn how to audit processes for effectiveness and efficiency.
You will learn an overview of the structure and content of ISO 9001:2015 and the contribution internal QMS audits can make to the effectiveness of your management system
This five (5) day, forty (40) hour, course provides participants with fundamental knowledge of assessment skills that will prepare participants to handle a variety of audit situations that add value to organizations. This course is certified (No. A18007) with the International Register of Certificated Auditors (IRCA) in the U.K. Successful completion of the course meets part of the formal training requirement for individuals seeking certification under the IRCA Auditor Registration Scheme.
Maximize your learning and your time when you take advantage of an additional day of insight through dynamic Audit and Business Improvement training as part of this select course package.
Why combine Problem Solving Tools & Techniques with Appreciation and New Quality Systems Manager? As a New Systems Manager, you need help you learning how to fulfil your role as a Systems Manager, how to form a robust system, plan and manage your internal audit activities, and implement effective corrective action....
Learn the essential elements a new Management Representative or Quality System Manager must know.
Maximize your learning and your time when you take advantage of an additional day of insight through dynamic Business Improvement training as part of this select course package.
You will learn what Annex SL is and how it is going to shape all ISO Standards published from now on. You will also learn the impact of Annex SL on the next revision of ISO 9001
Learn how to adapt your auditing technique to accommodate the new and amended requirements in ISO 9001:2015 and how to audit the new requirements concerning organizational context and the application of a risk-based approach.
This 8 – 12 hour course is for management systems managers and/or management representatives responsible for overseeing the transition. Learn about the potential impact of ISO 9001:2015 on your existing quality management system and how to smoothly address the required revisions.
Learn the structure of a generic management system based on Annex SL Appendix 2 and the implications of this from an audit perspective and the requirements for understanding the organization and its context and how they may be audited.
This course is a one-day add on to the ISO 9001:2015 Internal Auditor Transition course and delivered on-site.
This workshop contains the latest information on ISO 9001:2015 which signifies the first time all current and future users can access and review the proposed changes to ISO 9001, and is therefore in high-demand, so early registration is encouraged to secure your place.
Learn the concepts and requirements defined in ISO 9001:2015 and how they differ from ISO 9001:2008 and what needs to be revised in your current quality management system and how the new and enhanced requirements may be addressed.
Achieving certification to some of the world’s most widely-recognised international management system standards requires strategic planning, a strong internal team effort, coupled with a close working relationship with an independent and recognised provider of professional assurance services such as LRQA. These are just some of our clients whose achievements headlined last week.
US-based ASQ - the global knowledge network that links the best ideas, tools, and experts passionate about quality in more than 150 countries – has named LRQA’s Owen Ramsay as one of the 18 Fellows for his contribution and achievements within the quality arena. The new Fellows will be recognised at ASQ’s World Conference on Quality and Improvement in May.
SAN FRANCISCO, Calif. — Pacific Gas and Electric Company (PG&E) announced that Lloyd's Register Quality Assurance, an internationally-known independent management systems assurance firm, has certified the company's Supplier Quality Assurance Department's quality management system to the International Organization for Standardization (ISO) 9001:2008 standard.
Connect with us in Charlotte at the ASQ World Conference on Quality and Improvement. Visit us at stand #509 and discuss completing your transition to the revised standards.
LRQA's Medical Devices experts recently spoke at The Regulatory Affairs Professionals Society (RAPS) Regulatory Convergence. This annual event hosts the global regulatory community and brings together the profession’s best and brightest to learn, grow, lead and share.
Connect with us in Milwaukee at the ASQ World Conference on Quality and Improvement, there will be more than 100 sessions focusing on the 2016 theme—Quality Expanded: In the profession, through the organization, and around the world, ASQ World Conference on Quality.
Learn how compiling and maintaining product Technical Files/Design Dossiers in accordance with the European regulatory requirements can be administered while launching safe medical devices into the market in a timely and compliant manner.