Evolution of the Quality Management System - How to go from Surviving to Thriving

Added by globalcompliancepanel on 2018-01-04

Conference Dates:

Start Date Start Date: 2018-02-22
Last Date Last Day: 2018-02-23
Deadline for abstracts/proposals Deadline for abstracts/proposals: 2018-02-21

Conference Contact Info:

Contact Person Contact Person: Event manager
Email Email: [email protected]
Address Address: Los Angeles, Los Angeles, CA, United States
Phone Tel: 800-447-9407
Phone Fax: 302-288-6884

Conference Description:

Using lecture, discussion, and exercises, this 2 day seminar will focus on taking your QMS from surviving to thriving. We'll move from understanding the regulatory requirements, how to create your QMS structure, process thinking, and developing your improvement strategy. We'll discuss tools and techniques for improvement and how to measure your progress.

Why you should attend:
Many companies struggle to establish and maintain a Quality Management System (QMS) that is both efficient and effective. An ineffective QMS leads to disastrous consequences such as medical device reports, recalls, 483s, and warning letters. An ineffective QMS can result in serious consequences for your customers leading to dissatisfaction, serious injury, or even death. It is imperative that medical device companies can effectively establish a QMS.

And an inefficient QMS results in wasted time, money, and missed opportunities. In this 2-day seminar, we will use lecture, exercises, and discuss to learn the fundamentals of a Quality Management System and how you can take your program from surviving to thriving. A thriving QMS can help you achieve your compliance objectives and improve product quality, leading to higher customer satisfaction and business results.

Areas Covered in the Session:
Essentials of an effective QMS
Essentials of an efficient QMS
Quality is not an Organization
Key Capabilities
Maturity Modeling
Vision, Strategy, and Quality Planning
Improvement Tools
Best Practices
Who will benefit:
Quality Systems Specialists
Quality and Compliance Specialists
Auditors
Quality and Compliance Managers and Directors
CAPA Specialists
Project Managers
Supplier Quality Engineers and Auditors
Quality Engineers
Management Representatives
General Managers

Read More: http://www.globalcompliancepanel.com/con trol/globalseminars/~product_id=901489SE MINAR?worldconferencecalendar-February-2 018-SEO
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