Quality Risk Management Overview 2019

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Category Quality Professionals, Production Engineers, Production Supervisors

Deadline: May 01, 2019 | Date: May 02, 2019

Venue/Country: Online, U.S.A

Updated: 2019-03-20 15:06:00 (GMT+9)

Call For Papers - CFP

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: compliance4all14gmail.com