Date :
Place : United States, Jersey city
Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900601SEMINAR
Contact Person:Event Manager
Description:
In this seminar you will review all the quality management system requirements of FDA and ISO 13485 and then learn how to set up and manage an audit system that complies with these requirements, yet is risk-based so that your company makes the most efficient use of auditing resources for both internal and supplier audits. The seminar will include interactive exercises to reinforce the fundamentals of conducting and documenting quality system audits. Auditing principles taught in this seminar will be based on ISO 19011:2011 Guidelines for auditing management systems.Deadline for abstracts/proposals : 8th November 2016
Organized By :NetZealous LLC - GlobalCompliancePanel
Keynote Speakers : Betty Lane Founder and President, Be Quality Associates, LLC Betty Lane has over 30 years' experience in Medical Device quality assurance and regulatory affairs. She is the founder and President of Be Quality Associates, LLC, a consulting company helping small and medium sized medical device and diagnostic companies implement and improve their quality systems.
Conference Highlights :• Understand the basic requirements of FDA cGMP/ Quality System Regulation and ISO 13485 which are the basis for what must be audited in your internal audit program • Be able to develop or update and internal auditing system that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485, yet makes efficient use of company resources • Understand how to manage an Internal Audit system • Understand the difference between internal and external audits • Learn how the internal au
Venue :Courtyard Jersey City Newport, Washington Boulevard, Jersey City, NJ, United States
Check the event website for more details.