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2019 - Quality Risk Management Overview 2019

Date2019-05-02

Deadline2019-05-01

VenueFremont, USA - United States USA - United States

KeywordsMedical Devices; Risk management; Manufacturing

Websitehttps://www.compliance4all.com/control/w...

Topics/Call fo Papers

Overview:
Attendees will come away with the ability to recognize the purpose
and value of Quality Risk Management QRM.
Explain the level of risk based on severity, occurrence, and
detectability and how the QRM process is used to make decisions.
Why should you Attend:
It can provide a proactive approach to identifying, scientifically
evaluating and Controlling potential risks to quality
Integrating the principles of QRM into our quality processes is
complex especially in a pharmaceutical organization
Areas Covered in the Session:
Identify key QRM terminology
Identify examples of QRM tools and their application
Recognize the four (4) key components of Quality Risk Management
Who Will Benefit:
Process Owners
Quality Auditors
Quality Engineers
Quality Professionals
Production Engineers
Speaker Profile:
Steven Laurenz Chemical Engineering M.S. – Michigan State
University Expertise: Over 25 years of technical leadership
experience in product development, process development,
technology transfer, and process optimization. Skilled in taking new
products from early laboratory stage to successful manufacturing
launch.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14-AT-gmail.com

Last modified: 2019-03-14 15:42:13