2017 - Equipment and Facility Qualification 2017

Overview:
This webinar removes that confusion between equipment Qualification, process validation and Facility commissioning.
Why should you Attend:
The Webinar is designed for Quality and Manufacturing in the Pharmaceutical and Biopharmaceutical industries.
Areas Covered in the Session:
Quality Risk Management Defined
Compliance Requirements for Quality Risk Management
The Quality Risk Management Model
Quality Risk Management Life Cycle
Who Will Benefit:
Quality Engineers
Manufacturing Engineers
Line Managers
Speaker Profile:
Mr. Muchemu , MSc, MBA is the Co-founder and CEO of CGMP University Inc. Training and consulting organization in San Jose, California. Mister Muchemu is an established author of several GMP books. His background is Chemical Engineering. He has worked in the Pharmaceutical, Medical Device and Tissue industries for over fifteen years.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com