Lean Documents and Lean Configuration - 2017

Overview:  

The webinar will first present the key differences between ISO 13485 2015 versus ISO 13485 2003.Next, the speaker will provide an overview of the updated standard. 

Why should you Attend:

This webinar is an overview of the coming changes and their implications, using a new approach yet is based upon solid principles and proven practices. 

Areas Covered in the Session:

ISO 13485 2015 versus ISO 13485 2003

Overview of ISO 13485 2015

Systemic Requirements

Management Requirements

Resource Requirements

Realization Requirements

Remedial Requirements

Who Will Benefit:

Managers, Supervisors, Directors, and Vice-Presidents

R&D

Manufacturing Engineering

Design Assurance

Quality Assurance

Operations

Document Control

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: support@compliance4All.com

Speaker Profile: 

Jose Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device 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.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: support@compliance4All.com

Full Details & Registration Link: 
http://www.compliance4all.com/control/w_product/~product_id=501086LIVE?channel=mailer&camp=Webinar&AdGroup=ticketprinting_Apr_2017_SEO