Lloyd's Register: LR USA [ Change ]
866 971 5772
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.
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....
This two-day Medical Device Single Audit Program (MDSAP) is for medical device manufacturers who want to be audited only once for compliance with the standard and regulatory requirements of multiple regulatory authorities.
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.
This half day course promises to deliver an overview on the main areas of change and focus within ISO 9001:2015 and ISO 14001:2015. By looking at the impact Annex SL, the new high level structure for all management system standards, has had on the new standards, LRQA will discuss the new risk and leadership challenges and requirements and the enhanced elements for process management and performance evaluation.
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.
Trust is the focus of this year’s World Quality Day, which takes place on Thursday 8 November 2018. It is an opportunity to recognize the role that everyone in an organization plays in building and maintaining trust with stakeholders.
Achieving certification to some of the world’s most widely-recognized international management system standards requires strategic planning, a strong internal team effort, coupled with a close working relationship with an independent and recognized provider of professional assurance services such as Lloyd’s Register.
Over the last month, Lloyd’s Register has visited two yards and one sister company from Damen Shiprepair & Conversion’s (DSC) global network to audit their management systems.
Everyday leadership is the focus of this year’s World Quality Day, which will be celebrated on November 9, 2017. The Chartered Quality Institute (CQI) has put leadership at the core of its Competency Framework and highlights the leadership behaviors that quality professionals undertake in their daily work.
Achieving certification to some of the world’s most widely-recognized international management system standards requires strategic planning, a strong internal team effort, along with a close working relationship with an independent and recognized provider of professional assurance services such as LRQA.
Download the on-demand presentation with Susan discussing how to implement and maintain ISO 13485:2016 in order to help manufacturers ensure a successful transition to the revised standard.
Following an update previously released by UKAS, medical device manufacturers need to transition to the revised version of ISO 13485 by 31 March 2019. Considering that this deadline is fast approaching, medical device manufacturers have to plan and implement their transition. Lloyd’s Register (LR) is delivering a webinar on implementing and maintaining ISO 13485:2016 to help manufacturers ensure a successful implementation.
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.