ISO 13485 2016–Quality management systems - Requirements for regulatory purposes - By AtoZ Compliance

MessageThis Webinar is over
Date Apr 12, 2016
Time 01:00 PM EDT | 10:00 AM PDT
Cost $155.00
Online
Key Take Away

Learn how Medical device designers and manufacturers can follow ISO 13485 2016 to maintain their Quality Management System training (QMS) processes in a state of control, via controlled documents and objective evidence in the form of record keeping requirements.

Overview

All life science businesses are required to maintain their Quality Management System training (QMS) processes in a state of control, via controlled documents and objective evidence in the form of record keeping requirements. 
Medical device designers and manufacturers are required to follow ISO 13485 training, and will be expected to implement the 2016 revision changes. They will have the additional responsibility to ensure that each and every step of the manufacturing process is controlled by work instructions, SOP training, set-up instructions, equipment maintenance, and support functions, and that evidence of this work is maintained by controlled records.
The webinar will first present the key differences between ISO 13485 2016 versus ISO 13485 2003.
Next, the speaker will provide an overview of the updated standard.

Why Should You Attend

The changes to this standard will have profound implications to how Quality Management Systems (QMSs) interact internally and between different supply chain agents.
It would be a major oversight to think of these changes as anything but a game-changer in terms of expectations and requirements.
Rather than wait to be surprised by unexpected requirements, or to implement them haphazardly, it is better to understand what is coming and begin to plan for the changes that will permeate throughout all areas of your organization’s quality processes.
This webinar is an overview of the coming changes and their implications.

Areas Covered In This Webinar
  • ISO 13485 2016 versus ISO 13485 2003
Overview of ISO 13485 2016:
  • Systemic Requirements
  • Management Requirements
  • Resource Requirements
  • Realization Requirements
  • Remedial Requirements

Learning Objectives

Changes to ISO 13485 2016, although allowing more flexibility, introduces significant, comprehensive, and systemic changes involving the following areas:
  • Regulatory requirements
  • Risk-based approach
  • Medical device file
  • Record keeping
  • Product realization
  • User training
  • Design and development
  • Purchasing
  • Process validation guidance
  • Servicing
  • Complaints
  • Delivery of nonconforming product improvement

Who Will Benefit

Managers, Supervisors, Directors, and Vice-Presidents in the areas of:
  • R&D
  • Manufacturing Engineering
  • Design Assurance
  • Quality Assurance
  • Operations
  • Document Control

Speakers Profile

José Mora
José Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device and life sciences industry specializing in manufacturing, process development, tooling, and quality systems. Prior to working full time as a consulting partner for Atzari Consulting, José served as Director of Manufacturing Engineering at Boston Scientific and as Quality Systems Manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies. During that time he prepared a white paper on the application of lean manufacturing methods to the creation and management of controlled documents and a template for strategic deployment.
José led the launch of manufacturing at a start-up urology products company as Director of Manufacturing for UroSurge, Inc. at the University of Iowa's business incubator park in Coralville, IA, creating a world-class medical device manufacturing operation, with JIT, kanban systems, visual workplace and lean manufacturing practices.José worked for 10 years at Cordis Corporation, now a Johnson & Johnson company, where he led the successful tooling, process development and qualification of Cordis' first PTA (percutaneous transluminal angioplasty) catheter.
His medical device experience includes surgical instruments, PTA & PTCA dilatation and guiding catheters, plastic surgery implants and tissue expanders, urology implants and devices for the treatment of incontinence, delivery systems for brachytherapy, orthopaedic implants and instruments, and vascular surgery grafts and textiles. During his time at Cordis, José managed the Maintenance and Facilities Department, taking that operation to a level rated as "tops" by the UK Department of Health and Social Services (DHSS) during one of their intensive audits.
José managed Manufacturing Engineering as part of the Guiding Catheter Core Team of managers, a team that took the Cordis Guiding Catheter business to lead the market, bringing it up from fourth place. By introducing world-class techniques, the Guiding Catheter design and manufacturing was completely re-engineered for robust design and tooling, under José's leadership. He was also instrumental and played a leadership role in the complete re-engineering of the Tooling Control System, including design drafting, the tool shop and technical support. Wherever he has worked, he has a track record of introducing world-class methodologies such as Kepner-Tregoe, Taguchi techniques, Theory of Constraints, Lean Manufacturing, Five S (Visual Workplace), process validation to Global Harmonization Task Force standards, and similar approaches.

For more detail please click on this below link:

https://www.atozcompliance.com/trainings-webinar/life-sciences/medical-devices/iso-13485-2016-quality-management-systems-requirements-for-regulatory-purposes/jose-mora/300064

Email: referrals@atozcompliance.com
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Tel: +1-516-900-5509

 


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